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Published in: Orphanet Journal of Rare Diseases 1/2013

Open Access 01-12-2013 | Research

Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls

Authors: Anna E Hosman, Hannah L Devlin, B Maneesha Silva, Claire L Shovlin

Published in: Orphanet Journal of Rare Diseases | Issue 1/2013

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Abstract

Background

Hereditary haemorrhagic telangiectasia (HHT) is inherited as an autosomal dominant trait, affects ~1 in 5,000, and causes multi-systemic vascular lesions and life-limiting complications. Life expectancy is surprisingly good, particularly for patients over 60ys. We hypothesised that individuals with HHT may be protected against life-limiting cancers.

Methods

To compare specific cancer rates in HHT patients and controls, we developed a questionnaire capturing data on multiple relatives per respondent, powered to detect differences in the four most common solid non skin cancers (breast, colorectal, lung and prostate), each associated with significant mortality. Blinded to cancer responses, reports of HHT-specific features allowed assignment of participants and relatives as HHT-subjects, unknowns, or controls. Logistic and quadratic regressions were used to compare rates of specific cancer types between HHT subjects and controls.

Results

1,307 participants completed the questionnaire including 1,007 HHT-subjects and 142 controls. The rigorous HHT diagnostic algorithm meant that 158 (12%) completed datasets were not assignable either to HHT or control status. For cancers predominantly recognised as primary cancers, the rates in the controls generally matched age-standardised rates for the general population. HHT subjects recruited through the survey had similar demographics to controls, although the HHT group reported a significantly greater smoking habit. Combining data of participants and uniquely-reported relatives resulted in an HHT-arm of 2,161 (58% female), and control-arm of 2,817 (52% female), with median ages of 66ys [IQR 53–77] and 77ys [IQR 65–82] respectively. In both crude and age-adjusted regression, lung cancers were significantly less frequent in the HHT arm than controls (age-adjusted odds ratio 0.48 [0.30, 0.70], p = 0.0012). Breast cancer prevalence was higher in HHT than controls (age-adjusted OR 1.52 [1.07, 2.14], p = 0.018). Overall, prostate and colorectal cancer rates were equivalent, but the pattern of colorectal cancer was modified, with a higher prevalence in younger HHT patients than controls.

Conclusions

These preliminary survey data suggest clinically significant differences in the rates of lung, breast and colorectal cancer in HHT patients compared to controls. For rare diseases in which longitudinal studies take decades to recruit equivalent datasets, this type of methodology provides a good first-step method for data collection.
Appendix
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Literature
1.
go back to reference Kjeldsen AD, Vase P, Green A: Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients. J Intern Med. 1999, 245: 31-39. 10.1046/j.1365-2796.1999.00398.x.PubMedCrossRef Kjeldsen AD, Vase P, Green A: Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients. J Intern Med. 1999, 245: 31-39. 10.1046/j.1365-2796.1999.00398.x.PubMedCrossRef
2.
go back to reference Dakeishi M, Shioya T, Wada Y, Shindo T, Otaka K, Manabe M, Nozaki J, Inoue S, Koizumi A: Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan. Hum Mut. 2002, 19: 140-148. 10.1002/humu.10026.PubMedCrossRef Dakeishi M, Shioya T, Wada Y, Shindo T, Otaka K, Manabe M, Nozaki J, Inoue S, Koizumi A: Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan. Hum Mut. 2002, 19: 140-148. 10.1002/humu.10026.PubMedCrossRef
3.
go back to reference Plauchu H, de Chadarévian JP, Bideau A, Robert JM: Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. Am J Med Genet. 1989, 32 (3): 291-7. 10.1002/ajmg.1320320302.PubMedCrossRef Plauchu H, de Chadarévian JP, Bideau A, Robert JM: Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population. Am J Med Genet. 1989, 32 (3): 291-7. 10.1002/ajmg.1320320302.PubMedCrossRef
4.
go back to reference Govani FS, Shovlin CL: Hereditary haemorrhagic telangiectasia: a clinical and scientific review. Eur J Hum Genet. 2009, 17: 860-71. 10.1038/ejhg.2009.35.PubMedCentralPubMedCrossRef Govani FS, Shovlin CL: Hereditary haemorrhagic telangiectasia: a clinical and scientific review. Eur J Hum Genet. 2009, 17: 860-71. 10.1038/ejhg.2009.35.PubMedCentralPubMedCrossRef
5.
go back to reference Faughnan ME, Palda VA, Garcia-Tsao G, Geisthoff UW, McDonald J, Proctor DD, Spears J, Brown DH, Buscarini E, Chesnutt MS, Cottin V, Ganguly A, Gossage JR, Guttmacher AE, Hyland RH, Kennedy SJ, Korzenik J, Mager JJ, Ozanne AP, Piccirillo JF, Picus D, Plauchu H, Porteous ME, Pyeritz RE, Ross DA, Sabba C, Swanson K, Terry P, Wallace MC, Westermann CJ, White RI, Young LH, Zarrabeitia R: International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia. J Med Genet. 2011, 48: 73-87. 10.1136/jmg.2009.069013.PubMedCrossRef Faughnan ME, Palda VA, Garcia-Tsao G, Geisthoff UW, McDonald J, Proctor DD, Spears J, Brown DH, Buscarini E, Chesnutt MS, Cottin V, Ganguly A, Gossage JR, Guttmacher AE, Hyland RH, Kennedy SJ, Korzenik J, Mager JJ, Ozanne AP, Piccirillo JF, Picus D, Plauchu H, Porteous ME, Pyeritz RE, Ross DA, Sabba C, Swanson K, Terry P, Wallace MC, Westermann CJ, White RI, Young LH, Zarrabeitia R: International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia. J Med Genet. 2011, 48: 73-87. 10.1136/jmg.2009.069013.PubMedCrossRef
6.
go back to reference Shovlin CL: Hereditary hemorrhagic telangiectasia: pathophysiology, diagnosis and treatment. Blood Rev. 2010, 24: 203-19. 10.1016/j.blre.2010.07.001.PubMedCrossRef Shovlin CL: Hereditary hemorrhagic telangiectasia: pathophysiology, diagnosis and treatment. Blood Rev. 2010, 24: 203-19. 10.1016/j.blre.2010.07.001.PubMedCrossRef
7.
go back to reference Finnamore H, Le Couteur J, Hickson M, Busbridge M, Whelan K, Shovlin CL: Hemorrhage-adjusted iron requirements, hematinics and hepcidin define hereditary hemorrhagic telangiectasia as a model of hemorrhagic iron deficiency. PLoS ONE. 2013, 8 (10): e76516-10.1371/journal.pone.0076516.PubMedCentralPubMedCrossRef Finnamore H, Le Couteur J, Hickson M, Busbridge M, Whelan K, Shovlin CL: Hemorrhage-adjusted iron requirements, hematinics and hepcidin define hereditary hemorrhagic telangiectasia as a model of hemorrhagic iron deficiency. PLoS ONE. 2013, 8 (10): e76516-10.1371/journal.pone.0076516.PubMedCentralPubMedCrossRef
8.
go back to reference Kjeldsen A, Kjeldsen J: Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia. Am J Gastroenterol. 2000, 95: 415-8. 10.1111/j.1572-0241.2000.01792.x.PubMedCrossRef Kjeldsen A, Kjeldsen J: Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia. Am J Gastroenterol. 2000, 95: 415-8. 10.1111/j.1572-0241.2000.01792.x.PubMedCrossRef
9.
go back to reference Krings T, Ozanne A, Chng S, Alvarez H, Rodesch G, Lasjaunias P: Neurovascular phenotypes in hereditary haemorrhagic telangiectasia patients according to age. Review of 50 consecutive patients aged 1 day–60 years. Neuroradiology. 2005, 47: 711-20. 10.1007/s00234-005-1390-8.PubMedCrossRef Krings T, Ozanne A, Chng S, Alvarez H, Rodesch G, Lasjaunias P: Neurovascular phenotypes in hereditary haemorrhagic telangiectasia patients according to age. Review of 50 consecutive patients aged 1 day–60 years. Neuroradiology. 2005, 47: 711-20. 10.1007/s00234-005-1390-8.PubMedCrossRef
10.
go back to reference Shovlin CL, Jackson JE, Bamford KB, Jenkins IH, Benjamin AR, Ramadan H, Kulinskaya E: Primary determinants of ischemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia. Thorax. 2008, 63: 259-66. 10.1136/thx.2007.087452.PubMedCrossRef Shovlin CL, Jackson JE, Bamford KB, Jenkins IH, Benjamin AR, Ramadan H, Kulinskaya E: Primary determinants of ischemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia. Thorax. 2008, 63: 259-66. 10.1136/thx.2007.087452.PubMedCrossRef
11.
go back to reference Kjeldsen AD, Tørring PM, Nissen H, Andersen PE: Cerebral abscesses among Danish patients with hereditary haemorrhagic telangiectasia. Acta Neurol Scand. 2013, 10.1111/ane.12167. [Epub ahead of print] Kjeldsen AD, Tørring PM, Nissen H, Andersen PE: Cerebral abscesses among Danish patients with hereditary haemorrhagic telangiectasia. Acta Neurol Scand. 2013, 10.1111/ane.12167. [Epub ahead of print]
12.
go back to reference Hewes RC, Auster M, White RI: Cerebral embolism- first manifestation of pulmonary arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia. Cardiovasc Intervent Radiol. 1985, 8: 151-5. 10.1007/BF02552883.PubMedCrossRef Hewes RC, Auster M, White RI: Cerebral embolism- first manifestation of pulmonary arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia. Cardiovasc Intervent Radiol. 1985, 8: 151-5. 10.1007/BF02552883.PubMedCrossRef
13.
go back to reference Ference BA, Shannon TM, White RI Jr, Zawin M, Burdge CM: Life threatening pulmonary hemorrhage with pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia. Chest. 1994, 106: 1387-1392. 10.1378/chest.106.5.1387.PubMedCrossRef Ference BA, Shannon TM, White RI Jr, Zawin M, Burdge CM: Life threatening pulmonary hemorrhage with pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia. Chest. 1994, 106: 1387-1392. 10.1378/chest.106.5.1387.PubMedCrossRef
14.
go back to reference Shovlin CL, Sodhi V, McCarthy A, Lasjaunias P, Jackson JE, Sheppard MN: Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia suggested approach for obstetric services. BJOG. 2008, 115: 1108-15. 10.1111/j.1471-0528.2008.01786.x.PubMedCrossRef Shovlin CL, Sodhi V, McCarthy A, Lasjaunias P, Jackson JE, Sheppard MN: Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia suggested approach for obstetric services. BJOG. 2008, 115: 1108-15. 10.1111/j.1471-0528.2008.01786.x.PubMedCrossRef
15.
go back to reference Buscarini E, Leandro G, Conte D, Danesino C, Daina E, Manfredi G, Lupinacci G, Brambilla G, Menozzi F, De Grazia F, Gazzaniga P, Inama G, Bonardi R, Blotta P, Forner P, Olivieri C, Perna A, Grosso M, Pongiglione G, Boccardi E, Pagella F, Rossi G, Zambelli A: Natural history and outcome of hepatic vascular malformations in a large cohort of patients with hereditary hemorrhagic telangiectasia. Dig Dis Sci. 2011, 56 (7): 2166-78. 10.1007/s10620-011-1585-2.PubMedCentralPubMedCrossRef Buscarini E, Leandro G, Conte D, Danesino C, Daina E, Manfredi G, Lupinacci G, Brambilla G, Menozzi F, De Grazia F, Gazzaniga P, Inama G, Bonardi R, Blotta P, Forner P, Olivieri C, Perna A, Grosso M, Pongiglione G, Boccardi E, Pagella F, Rossi G, Zambelli A: Natural history and outcome of hepatic vascular malformations in a large cohort of patients with hereditary hemorrhagic telangiectasia. Dig Dis Sci. 2011, 56 (7): 2166-78. 10.1007/s10620-011-1585-2.PubMedCentralPubMedCrossRef
16.
go back to reference Lerut J, Orlando G, Adam R, Sabbà C, Pfitzmann R, Klempnauer J, Belghiti J, Pirenne J, Thevenot T, Hillert C, Brown CM, Gonze D, Karam V, Boillot O: European Liver Transplant Association. Liver transplantation for hereditary hemorrhagic telangiectasia: report of the European liver transplant registry. Ann Surg. 2006, 244: 854-62. 10.1097/01.sla.0000247258.35406.a4.PubMedCentralPubMedCrossRef Lerut J, Orlando G, Adam R, Sabbà C, Pfitzmann R, Klempnauer J, Belghiti J, Pirenne J, Thevenot T, Hillert C, Brown CM, Gonze D, Karam V, Boillot O: European Liver Transplant Association. Liver transplantation for hereditary hemorrhagic telangiectasia: report of the European liver transplant registry. Ann Surg. 2006, 244: 854-62. 10.1097/01.sla.0000247258.35406.a4.PubMedCentralPubMedCrossRef
17.
go back to reference Girerd B, Montani D, Coulet F, Sztrymf B, Yaici A, Jaïs X, Tregouet D, Reis A, Drouin-Garraud V, Fraisse A, Sitbon O, O'Callaghan DS, Simonneau G, Soubrier F, Humbert M: Clinical outcomes of pulmonary arterial hypertension in patients carrying an ACVRL1 (ALK1) mutation. Am J Respir Crit Care Med. 2010, 181: 851-61. 10.1164/rccm.200908-1284OC.PubMedCrossRef Girerd B, Montani D, Coulet F, Sztrymf B, Yaici A, Jaïs X, Tregouet D, Reis A, Drouin-Garraud V, Fraisse A, Sitbon O, O'Callaghan DS, Simonneau G, Soubrier F, Humbert M: Clinical outcomes of pulmonary arterial hypertension in patients carrying an ACVRL1 (ALK1) mutation. Am J Respir Crit Care Med. 2010, 181: 851-61. 10.1164/rccm.200908-1284OC.PubMedCrossRef
18.
go back to reference Shovlin CL, Sulainam NL, Govani FS, Jackson JE, Begbie ME: Elevated Factor VIII in hereditary haemorrhagic telangiectasia (HHT): association with venous thromboembolism. Thromb Haemost. 2007, 98: 1031-9.PubMed Shovlin CL, Sulainam NL, Govani FS, Jackson JE, Begbie ME: Elevated Factor VIII in hereditary haemorrhagic telangiectasia (HHT): association with venous thromboembolism. Thromb Haemost. 2007, 98: 1031-9.PubMed
19.
go back to reference Livesey JA, Manning R, Meek JH, Jackson JE, Kulinskaya E, Laffan MA, Shovlin CL: Low serum iron levels are associated with elevated plasma levels of coagulation factor VIII and pulmonary emboli/deep venous thromboses in replicate cohorts of patients with hereditary hemorrhagic telangiectasia. Thorax. 2012, 67: 328-33. 10.1136/thoraxjnl-2011-201076.PubMedCrossRef Livesey JA, Manning R, Meek JH, Jackson JE, Kulinskaya E, Laffan MA, Shovlin CL: Low serum iron levels are associated with elevated plasma levels of coagulation factor VIII and pulmonary emboli/deep venous thromboses in replicate cohorts of patients with hereditary hemorrhagic telangiectasia. Thorax. 2012, 67: 328-33. 10.1136/thoraxjnl-2011-201076.PubMedCrossRef
20.
go back to reference Brosens LA, van Hattem A, Hylind LM, Iacobuzio-Donahue C, Romans KE, Axilbund J, Cruz-Correa M, Tersmette AC, Offerhaus GJ, Giardiello FM: Risk of colorectal cancer in juvenile polyposis. Gut. 2007, 56: 965-7. 10.1136/gut.2006.116913.PubMedCentralPubMedCrossRef Brosens LA, van Hattem A, Hylind LM, Iacobuzio-Donahue C, Romans KE, Axilbund J, Cruz-Correa M, Tersmette AC, Offerhaus GJ, Giardiello FM: Risk of colorectal cancer in juvenile polyposis. Gut. 2007, 56: 965-7. 10.1136/gut.2006.116913.PubMedCentralPubMedCrossRef
21.
go back to reference Schwenter F, Faughnan ME, Gradinger AB, Berk T, Gryfe R, Pollett A, Cohen Z, Gallinger S, Durno C: Juvenile polyposis, hereditary hemorrhagic telangiectasia, and early onset colorectal cancer in patients with SMAD4 mutation. J Gastroenterol. 2012, 47: 795-804. 10.1007/s00535-012-0545-8.PubMedCrossRef Schwenter F, Faughnan ME, Gradinger AB, Berk T, Gryfe R, Pollett A, Cohen Z, Gallinger S, Durno C: Juvenile polyposis, hereditary hemorrhagic telangiectasia, and early onset colorectal cancer in patients with SMAD4 mutation. J Gastroenterol. 2012, 47: 795-804. 10.1007/s00535-012-0545-8.PubMedCrossRef
22.
go back to reference Devlin HL, Hosman AE, Shovlin CL: Antiplatelets and anticoagulants in hereditary hemorrhagic telangiectasia. New Engl J Med. 2013, 368: 876-8. 10.1056/NEJMc1213554.PubMedCrossRef Devlin HL, Hosman AE, Shovlin CL: Antiplatelets and anticoagulants in hereditary hemorrhagic telangiectasia. New Engl J Med. 2013, 368: 876-8. 10.1056/NEJMc1213554.PubMedCrossRef
23.
go back to reference Sabbà C, Pasculli G, Suppressa P, D'Ovidio F, Lenato GM, Resta F, Assennato G, Guanti G: Life expectancy in patients with hereditary haemorrhagic telangiectasia. QJM. 2006, 99: 327-34. 10.1093/qjmed/hcl037.PubMedCrossRef Sabbà C, Pasculli G, Suppressa P, D'Ovidio F, Lenato GM, Resta F, Assennato G, Guanti G: Life expectancy in patients with hereditary haemorrhagic telangiectasia. QJM. 2006, 99: 327-34. 10.1093/qjmed/hcl037.PubMedCrossRef
24.
go back to reference de Gussem EM, Edwards CP, Westermann CJJ, Faughnan ME, Mager JJ: Life expectancy of parents with hereditary hemorrhagic telangiectasia. Hematol Meet Rep. 2009, 3 (Suppl 4): 11-2. de Gussem EM, Edwards CP, Westermann CJJ, Faughnan ME, Mager JJ: Life expectancy of parents with hereditary hemorrhagic telangiectasia. Hematol Meet Rep. 2009, 3 (Suppl 4): 11-2.
25.
go back to reference Goodwin J, Nisenbaum R, Edwards C, Faughnan ME: Survival in hereditary hemorrhagic telangiectasia. Hematol Meet Rep. 2009, 3 (Suppl 4): 12. Goodwin J, Nisenbaum R, Edwards C, Faughnan ME: Survival in hereditary hemorrhagic telangiectasia. Hematol Meet Rep. 2009, 3 (Suppl 4): 12.
26.
go back to reference Guttmacher AE, McKinnon WC, Taylor LA, Berg J, Porteous MEM, Korsenik J, Fayad PB, Shovlin C, Burdge CM, Jacobson B, Van Cutsem E, Westermann CJJ, Kjeldsen A, Vase P, White RI, McDonald J, Marchuk DA: The natural history of hereditary haemorrhagic telangiectasia: data from a patient questionnaire. 1997, Curaçao: Conference Proceedings for HHT Foundation Int., Scientific Meeting Guttmacher AE, McKinnon WC, Taylor LA, Berg J, Porteous MEM, Korsenik J, Fayad PB, Shovlin C, Burdge CM, Jacobson B, Van Cutsem E, Westermann CJJ, Kjeldsen A, Vase P, White RI, McDonald J, Marchuk DA: The natural history of hereditary haemorrhagic telangiectasia: data from a patient questionnaire. 1997, Curaçao: Conference Proceedings for HHT Foundation Int., Scientific Meeting
29.
go back to reference Easey AJ, Wallace GM, Hughes JM, Jackson JE, Taylor WJ, Shovlin CL: Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life. J Neurol Neurosurg Psych. 2003, 74: 743-8. 10.1136/jnnp.74.6.743.CrossRef Easey AJ, Wallace GM, Hughes JM, Jackson JE, Taylor WJ, Shovlin CL: Should asymptomatic patients with hereditary haemorrhagic telangiectasia (HHT) be screened for cerebral vascular malformations? Data from 22,061 years of HHT patient life. J Neurol Neurosurg Psych. 2003, 74: 743-8. 10.1136/jnnp.74.6.743.CrossRef
30.
go back to reference Silva BM, Hosman AE, Devlin HL, Shovlin CL: A questionnaire-based study suggests lifestyle and dietary factors influencing nosebleed severity in hereditary hemorrhagic telangiectasia (HHT). Laryngoscope. 2013, 123: 1092-9. 10.1002/lary.23893.PubMedCrossRef Silva BM, Hosman AE, Devlin HL, Shovlin CL: A questionnaire-based study suggests lifestyle and dietary factors influencing nosebleed severity in hereditary hemorrhagic telangiectasia (HHT). Laryngoscope. 2013, 123: 1092-9. 10.1002/lary.23893.PubMedCrossRef
32.
go back to reference Shovlin CL, Guttmacher AE, Buscarini E, Faughan M, Hyland R, Westermann CJJ, Plauchu H: Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet. 2000, 91: 66-7. 10.1002/(SICI)1096-8628(20000306)91:1<66::AID-AJMG12>3.0.CO;2-P.PubMedCrossRef Shovlin CL, Guttmacher AE, Buscarini E, Faughan M, Hyland R, Westermann CJJ, Plauchu H: Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet. 2000, 91: 66-7. 10.1002/(SICI)1096-8628(20000306)91:1<66::AID-AJMG12>3.0.CO;2-P.PubMedCrossRef
33.
go back to reference van Gent MW, Velthuis S, Post MC, Snijder RJ, Westermann CJ, Letteboer TG, Mager JJ: Hereditary hemorrhagic telangiectasia: how accurate are the clinical criteria?. Am J Med Genet A. 2013, 161: 461-6. 10.1002/ajmg.a.35715.CrossRef van Gent MW, Velthuis S, Post MC, Snijder RJ, Westermann CJ, Letteboer TG, Mager JJ: Hereditary hemorrhagic telangiectasia: how accurate are the clinical criteria?. Am J Med Genet A. 2013, 161: 461-6. 10.1002/ajmg.a.35715.CrossRef
35.
go back to reference Govani FS, Giess A, Mollet IM, Begbie ME, Jones M, Game L, Shovlin CL: Directional next-generation RNA sequencing and examination of premature termination codon mutations in endoglin/hereditary haemorrhagic telangiectasia. Mol Syndromol. 2013, 4: 184-196. 10.1159/000350208.PubMedCentralPubMedCrossRef Govani FS, Giess A, Mollet IM, Begbie ME, Jones M, Game L, Shovlin CL: Directional next-generation RNA sequencing and examination of premature termination codon mutations in endoglin/hereditary haemorrhagic telangiectasia. Mol Syndromol. 2013, 4: 184-196. 10.1159/000350208.PubMedCentralPubMedCrossRef
36.
go back to reference McDonald J, Gedge F, Burdette A, Carlisle J, Bukjiok C, et al, et al: Multiple sequence variants in hereditary hemorrhagic telangiectasia cases: illustration of complexity in molecular diagnostic interpretation. J Mol Diagnostics. 2009, 11 (6): 569-575. 10.2353/jmoldx.2009.080148.CrossRef McDonald J, Gedge F, Burdette A, Carlisle J, Bukjiok C, et al, et al: Multiple sequence variants in hereditary hemorrhagic telangiectasia cases: illustration of complexity in molecular diagnostic interpretation. J Mol Diagnostics. 2009, 11 (6): 569-575. 10.2353/jmoldx.2009.080148.CrossRef
37.
go back to reference Pece N, Vera S, Cymerman U, White R, Wrana J, Letarte M: Mutant endoglin in Hereditary Hemorrhagic Telangiectasia type I is transiently expressed intracellularly and is not a dominant negative. J Clin Invest. 1997, 100: 2568-2579. 10.1172/JCI119800.PubMedCentralPubMedCrossRef Pece N, Vera S, Cymerman U, White R, Wrana J, Letarte M: Mutant endoglin in Hereditary Hemorrhagic Telangiectasia type I is transiently expressed intracellularly and is not a dominant negative. J Clin Invest. 1997, 100: 2568-2579. 10.1172/JCI119800.PubMedCentralPubMedCrossRef
38.
go back to reference Pece-Barbara N, Cymerman U, Vera S, Marchuk D, Letarte M: Expression analysis of four endoglin missense mutations suggests haploinsufficiency is the predominant mechanism for Hereditary Hemorrhagic Telangiectasia type I. Hum Mol Genet. 1999, 8: 2171-2181. 10.1093/hmg/8.12.2171.PubMedCrossRef Pece-Barbara N, Cymerman U, Vera S, Marchuk D, Letarte M: Expression analysis of four endoglin missense mutations suggests haploinsufficiency is the predominant mechanism for Hereditary Hemorrhagic Telangiectasia type I. Hum Mol Genet. 1999, 8: 2171-2181. 10.1093/hmg/8.12.2171.PubMedCrossRef
39.
go back to reference Pece-Barbara N, Vera S, Kathirkamathamby K, Liebner S, Di Guglielmo GM, Dejana E, Wrana JL, Letarte M: Endoglin null endothelial cells proliferate faster and are more responsive to transforming growth factor beta1 with higher affinity receptors and an activated Alk1 pathway. J Biol Chem. 2005, 280: 27800-27808. 10.1074/jbc.M503471200.PubMedCrossRef Pece-Barbara N, Vera S, Kathirkamathamby K, Liebner S, Di Guglielmo GM, Dejana E, Wrana JL, Letarte M: Endoglin null endothelial cells proliferate faster and are more responsive to transforming growth factor beta1 with higher affinity receptors and an activated Alk1 pathway. J Biol Chem. 2005, 280: 27800-27808. 10.1074/jbc.M503471200.PubMedCrossRef
40.
go back to reference Bourdeau A, Cymerman U, Paquet ME, Meschino W, McKinnon WC, Guttmacher AE, Becker L, Letarte M: Endoglin expression is reduced in normal vessels but still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type 1. Am J Pathol. 2000, 156: 911-923. 10.1016/S0002-9440(10)64960-7.PubMedCentralPubMedCrossRef Bourdeau A, Cymerman U, Paquet ME, Meschino W, McKinnon WC, Guttmacher AE, Becker L, Letarte M: Endoglin expression is reduced in normal vessels but still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type 1. Am J Pathol. 2000, 156: 911-923. 10.1016/S0002-9440(10)64960-7.PubMedCentralPubMedCrossRef
41.
go back to reference Cymerman U, Vera S, Pece-Barbara N, Bourdeau A, White RI Jr, Dunn J, Letarte M: Identification of Hereditary Hemorrhagic Telangiectasia type I in newborns by protein expression and mutation analysis of endoglin. Pediatr Res. 2000, 47: 24-35. 10.1203/00006450-200001000-00008.PubMedCrossRef Cymerman U, Vera S, Pece-Barbara N, Bourdeau A, White RI Jr, Dunn J, Letarte M: Identification of Hereditary Hemorrhagic Telangiectasia type I in newborns by protein expression and mutation analysis of endoglin. Pediatr Res. 2000, 47: 24-35. 10.1203/00006450-200001000-00008.PubMedCrossRef
42.
go back to reference Paquet ME, Pece-Barbara N, Vera S, Cymerman U, Karabegovic A, Shovlin C, Letarte M: Analysis of several endoglin mutants reveals no endogenous mature or secreted protein capable of interfering with normal endoglin function. Hum Mol Genet. 2001, 10: 1347-1357. 10.1093/hmg/10.13.1347.PubMedCrossRef Paquet ME, Pece-Barbara N, Vera S, Cymerman U, Karabegovic A, Shovlin C, Letarte M: Analysis of several endoglin mutants reveals no endogenous mature or secreted protein capable of interfering with normal endoglin function. Hum Mol Genet. 2001, 10: 1347-1357. 10.1093/hmg/10.13.1347.PubMedCrossRef
43.
go back to reference Fernandez-L A, Sanz-Rodriguez F, Zarrabeitia R, Perez-Molino A, Morales C, Restrepo CM, Ramirez JR, Coto E, Lenato GM, Bernabeu C, Botella LM: Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1. Hum Mutat. 2006, 27: 295.PubMedCrossRef Fernandez-L A, Sanz-Rodriguez F, Zarrabeitia R, Perez-Molino A, Morales C, Restrepo CM, Ramirez JR, Coto E, Lenato GM, Bernabeu C, Botella LM: Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of Endoglin and ALK1. Hum Mutat. 2006, 27: 295.PubMedCrossRef
44.
go back to reference Seki T, Yun J, Oh SP: Arterial endothelium-specific activin receptor- like kinase 1 expression suggests its role in arterialization and vascular remodeling. Circ Res. 2003, 93: 682-9. 10.1161/01.RES.0000095246.40391.3B.PubMedCrossRef Seki T, Yun J, Oh SP: Arterial endothelium-specific activin receptor- like kinase 1 expression suggests its role in arterialization and vascular remodeling. Circ Res. 2003, 93: 682-9. 10.1161/01.RES.0000095246.40391.3B.PubMedCrossRef
45.
go back to reference Santibanez JF, Pérez-Gómez E, Fernandez-L A, Garrido-Martin EM, Carnero A, Malumbres M, Vary CP, Quintanilla M, Bernabéu C: The TGF-beta co-receptor endoglin modulates the expression and transforming potential of H-Ras. Carcinogenesis. 2010, 31: 2145-54. 10.1093/carcin/bgq199.PubMedCrossRef Santibanez JF, Pérez-Gómez E, Fernandez-L A, Garrido-Martin EM, Carnero A, Malumbres M, Vary CP, Quintanilla M, Bernabéu C: The TGF-beta co-receptor endoglin modulates the expression and transforming potential of H-Ras. Carcinogenesis. 2010, 31: 2145-54. 10.1093/carcin/bgq199.PubMedCrossRef
46.
go back to reference Ziebarth AJ, Nowsheen S, Steg AD, Shah MM, Katre AA, Dobbin ZC, Han HD, Lopez-Berestein G, Sood AK, Conner M, Yang ES, Landen CN: Endoglin (CD105) contributes to platinum resistance and is a target for tumor-specific therapy in epithelial ovarian cancer. Clin Cancer Res. 2013, 19: 170-82. 10.1158/1078-0432.CCR-12-1045.PubMedCentralPubMedCrossRef Ziebarth AJ, Nowsheen S, Steg AD, Shah MM, Katre AA, Dobbin ZC, Han HD, Lopez-Berestein G, Sood AK, Conner M, Yang ES, Landen CN: Endoglin (CD105) contributes to platinum resistance and is a target for tumor-specific therapy in epithelial ovarian cancer. Clin Cancer Res. 2013, 19: 170-82. 10.1158/1078-0432.CCR-12-1045.PubMedCentralPubMedCrossRef
47.
go back to reference Uneda S, Toi H, Tsujie T, Tsujie M, Harada N, Tsai H, Seon BK: Anti-endoglin monoclonal antibodies are effective for suppressing metastasis and the primary tumors by targeting tumor vasculature. Int J Cancer. 2009, 125: 1446-53. 10.1002/ijc.24482.PubMedCentralPubMedCrossRef Uneda S, Toi H, Tsujie T, Tsujie M, Harada N, Tsai H, Seon BK: Anti-endoglin monoclonal antibodies are effective for suppressing metastasis and the primary tumors by targeting tumor vasculature. Int J Cancer. 2009, 125: 1446-53. 10.1002/ijc.24482.PubMedCentralPubMedCrossRef
48.
go back to reference van Meeteren LA, Thorikay M, Bergqvist S, Pardali E, Stampino CG, Hu-Lowe D, Goumans MJ, ten Dijke P: Anti-human activin receptor-like kinase 1 (ALK1) antibody attenuates bone morphogenetic protein 9 (BMP9)-induced ALK1 signaling and interferes with endothelial cell sprouting. J Biol Chem. 2012, 287: 18551-61. 10.1074/jbc.M111.338103.PubMedCentralPubMedCrossRef van Meeteren LA, Thorikay M, Bergqvist S, Pardali E, Stampino CG, Hu-Lowe D, Goumans MJ, ten Dijke P: Anti-human activin receptor-like kinase 1 (ALK1) antibody attenuates bone morphogenetic protein 9 (BMP9)-induced ALK1 signaling and interferes with endothelial cell sprouting. J Biol Chem. 2012, 287: 18551-61. 10.1074/jbc.M111.338103.PubMedCentralPubMedCrossRef
49.
go back to reference Anderberg C, Cunha SI, Zhai Z, Cortez E, Pardali E, Johnson JR, Franco M, Páez-Ribes M, Cordiner R, Fuxe J, Johansson BR, Goumans MJ, Casanovas O, ten Dijke P, Arthur HM, Pietras K: Deficiency for endoglin in tumor vasculature weakens the endothelial barrier to metastatic dissemination. J Exp Med. 2013, 210: 563-79. 10.1084/jem.20120662.PubMedCentralPubMedCrossRef Anderberg C, Cunha SI, Zhai Z, Cortez E, Pardali E, Johnson JR, Franco M, Páez-Ribes M, Cordiner R, Fuxe J, Johansson BR, Goumans MJ, Casanovas O, ten Dijke P, Arthur HM, Pietras K: Deficiency for endoglin in tumor vasculature weakens the endothelial barrier to metastatic dissemination. J Exp Med. 2013, 210: 563-79. 10.1084/jem.20120662.PubMedCentralPubMedCrossRef
50.
go back to reference Henry LA, Johnson DA, Sarrió D, Lee S, Quinlan PR, Crook T, Thompson AM, Reis-Filho JS, Isacke CM: Endoglin expression in breast tumor cells suppresses invasion and metastasis and correlates with improved clinical outcome. Oncogene. 2011, 30: 1046-58. 10.1038/onc.2010.488.PubMedCrossRef Henry LA, Johnson DA, Sarrió D, Lee S, Quinlan PR, Crook T, Thompson AM, Reis-Filho JS, Isacke CM: Endoglin expression in breast tumor cells suppresses invasion and metastasis and correlates with improved clinical outcome. Oncogene. 2011, 30: 1046-58. 10.1038/onc.2010.488.PubMedCrossRef
51.
go back to reference Quintanilla M, Ramirez JR, Pérez-Gómez E, Romero D, Velasco B, Letarte M, López-Novoa JM, Bernabéu C: Expression of the TGF-beta coreceptor endoglin in epidermal keratinocytes and its dual role in multistage mouse skin carcinogenesis. Oncogene. 2003, 22: 5976-5985. 10.1038/sj.onc.1206841.PubMedCrossRef Quintanilla M, Ramirez JR, Pérez-Gómez E, Romero D, Velasco B, Letarte M, López-Novoa JM, Bernabéu C: Expression of the TGF-beta coreceptor endoglin in epidermal keratinocytes and its dual role in multistage mouse skin carcinogenesis. Oncogene. 2003, 22: 5976-5985. 10.1038/sj.onc.1206841.PubMedCrossRef
52.
go back to reference Jerkic M, Rodríguez-Barbero A, Prieto M, Toporsian M, Pericacho M, Rivas-Elena JV, Obreo J, Wang A, Pérez-Barriocanal F, Arévalo M, Bernabéu C, Letarte M, López-Novoa JM: Reduced angiogenic responses in adult Endoglin heterozygous mice. Cardiovasc Res. 2006, 69: 845-54. 10.1016/j.cardiores.2005.11.020.PubMedCrossRef Jerkic M, Rodríguez-Barbero A, Prieto M, Toporsian M, Pericacho M, Rivas-Elena JV, Obreo J, Wang A, Pérez-Barriocanal F, Arévalo M, Bernabéu C, Letarte M, López-Novoa JM: Reduced angiogenic responses in adult Endoglin heterozygous mice. Cardiovasc Res. 2006, 69: 845-54. 10.1016/j.cardiores.2005.11.020.PubMedCrossRef
53.
go back to reference Mitchell D, Pobre EG, Mulivor AW, Grinberg AV, Castonguay R, Monnell TE, Solban N, Ucran JA, Pearsall RS, Underwood KW, Seehra J, Kumar R: ALK1-Fc Inhibits Multiple Mediators of Angiogenesis and Suppresses Tumor Growth. Mol Cancer Ther. 2010, 9: 379-388. 10.1158/1535-7163.MCT-09-0650.PubMedCrossRef Mitchell D, Pobre EG, Mulivor AW, Grinberg AV, Castonguay R, Monnell TE, Solban N, Ucran JA, Pearsall RS, Underwood KW, Seehra J, Kumar R: ALK1-Fc Inhibits Multiple Mediators of Angiogenesis and Suppresses Tumor Growth. Mol Cancer Ther. 2010, 9: 379-388. 10.1158/1535-7163.MCT-09-0650.PubMedCrossRef
54.
go back to reference Rosen LS, Hurwitz HI, Wong MK, Goldman J, Mendelson DS, Figg WD, Spencer S, Adams BJ, Alvarez D, Seon BK, Theuer CP, Leigh BR, Gordon MS: A phase I first-in-human study of TRC105 (Anti-Endoglin Antibody) in patients with advanced cancer. Clin Cancer Res. 2012, 18: 4820-9. 10.1158/1078-0432.CCR-12-0098.PubMedCentralPubMedCrossRef Rosen LS, Hurwitz HI, Wong MK, Goldman J, Mendelson DS, Figg WD, Spencer S, Adams BJ, Alvarez D, Seon BK, Theuer CP, Leigh BR, Gordon MS: A phase I first-in-human study of TRC105 (Anti-Endoglin Antibody) in patients with advanced cancer. Clin Cancer Res. 2012, 18: 4820-9. 10.1158/1078-0432.CCR-12-0098.PubMedCentralPubMedCrossRef
56.
go back to reference Elphick A, Shovlin CL: Relationships between epistaxis, migraines, and triggers in hereditary hemorrhagic telangiectasia. Laryngoscope. 2013, 10.1002/lary.24526 Elphick A, Shovlin CL: Relationships between epistaxis, migraines, and triggers in hereditary hemorrhagic telangiectasia. Laryngoscope. 2013, 10.1002/lary.24526
57.
go back to reference Berrington De González A, Darby S: Risk of cancer from diagnostic X-rays: estimates for the UK and 14 other countries. Lancet. 2004, 363: 345-51. 10.1016/S0140-6736(04)15433-0.PubMedCrossRef Berrington De González A, Darby S: Risk of cancer from diagnostic X-rays: estimates for the UK and 14 other countries. Lancet. 2004, 363: 345-51. 10.1016/S0140-6736(04)15433-0.PubMedCrossRef
58.
go back to reference Chodick G, Ronckers C, Shalev V, Ron E: Excess lifetime cancer mortality risk attributable to radiation exposure from computed tomography examinations in children. Isr Med Assoc J. 2007, 9: 584-7.PubMed Chodick G, Ronckers C, Shalev V, Ron E: Excess lifetime cancer mortality risk attributable to radiation exposure from computed tomography examinations in children. Isr Med Assoc J. 2007, 9: 584-7.PubMed
59.
go back to reference Rice H, Frush D, Farmer D, Waldhausen J: APSA Education Committee Review of radiation risks from computed tomography: essentials for the pediatric surgeon. J Pediatr Surg. 2007, 42: 603-7. 10.1016/j.jpedsurg.2006.12.009.PubMedCrossRef Rice H, Frush D, Farmer D, Waldhausen J: APSA Education Committee Review of radiation risks from computed tomography: essentials for the pediatric surgeon. J Pediatr Surg. 2007, 42: 603-7. 10.1016/j.jpedsurg.2006.12.009.PubMedCrossRef
60.
go back to reference Thierry-Chef I, Simon SL, Land CE, Miller DL: Radiation dose to the brain and subsequent risk of developing brain tumors in pediatric patients undergoing interventional neuroradiology procedures. Radiat Res. 2008, 170: 553-65. 10.1667/RR1393.1.PubMedCentralPubMedCrossRef Thierry-Chef I, Simon SL, Land CE, Miller DL: Radiation dose to the brain and subsequent risk of developing brain tumors in pediatric patients undergoing interventional neuroradiology procedures. Radiat Res. 2008, 170: 553-65. 10.1667/RR1393.1.PubMedCentralPubMedCrossRef
61.
go back to reference Ma S, Kong B, Liu B, Liu X: Biological effects of low-dose radiation from computed tomography scanning. Int J Radiat Biol. 2013, 89: 326-33. 10.3109/09553002.2013.756595.PubMedCrossRef Ma S, Kong B, Liu B, Liu X: Biological effects of low-dose radiation from computed tomography scanning. Int J Radiat Biol. 2013, 89: 326-33. 10.3109/09553002.2013.756595.PubMedCrossRef
Metadata
Title
Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls
Authors
Anna E Hosman
Hannah L Devlin
B Maneesha Silva
Claire L Shovlin
Publication date
01-12-2013
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2013
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/1750-1172-8-195

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