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Published in: Hereditary Cancer in Clinical Practice 1/2017

Open Access 01-12-2017 | Review

ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis

Authors: Yan Jiang, Chen-Yang Zhao, Li-Chun Cheng, Bing Xu, Hui-Yi Lv

Published in: Hereditary Cancer in Clinical Practice | Issue 1/2017

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Abstract

Adenosine diphosphate (ADP)-ribosylation factor-like tumour suppressor gene 1(ARLTS1) might be associated with an increased risk of several types of familial cancers. However, previous studies have shown that cancer susceptibility is not completely consistent with ARLTS1 polymorphisms, and the precise mechanism remains unknown. Therefore, we conducted a meta-analysis of case-control studies by searching the PubMed, Embase, OVID, Science Direct and Chinese National Knowledge Infrastructure (CNKI) databases. In total, 12 studies met the inclusion criteria and were included in this meta-analysis. Statistical analyses were performed using STATA 11.0 software. Overall, the Cys148Arg T > C variant significantly increased cancer risk (CC vs. TT: OR = 1.27, 95% CI = 1.15–1.41, P < 0.05). The stratification indicated that the Cys148Arg variant is significantly associated with sporadic cancer (CC vs. TT: OR = 1.36, 95% CI = 1.18–1.55) and familial cancer (CC vs. TT: OR = 1.26, 95% CI = 1.12–1.43). Trp149Stop, Pro131Leu, Ser99Ser and Leu132Leu were not correlated with cancer susceptibility. Based on these results, we demonstrated that the ARLTS1 Cys148Arg polymorphism is associated with an increased risk of sporadic cancer and familial cancer, and there were no associations between the other four SNPs (i.e., Trp149Stop, Pro131Leu, Ser99Ser and Leu132Leu) and cancer risk.
Literature
1.
2.
go back to reference Calin GA, Trapasso F, Shimizu M, Dumitru CD, Yendamuri S, Godwin AK, Ferracin M, Bernardi G, Chatterjee D, Baldassarre G, Rattan S, Alder H, Mabuchi H, Shiraishi T, Hansen LL, Overgaard J, Herlea V, Mauro FR, Dighiero G, Movsas B, Rassenti L, Kipps T, Baffa R, Fusco A, Mori M, Russo G, Liu CG, Neuberg D, Bullrich F, Negrini M, Croce CM. Familial cancer associated with a polymorphism in ARLTS1. N Engl J Med. 2005;352:1667–76.CrossRefPubMed Calin GA, Trapasso F, Shimizu M, Dumitru CD, Yendamuri S, Godwin AK, Ferracin M, Bernardi G, Chatterjee D, Baldassarre G, Rattan S, Alder H, Mabuchi H, Shiraishi T, Hansen LL, Overgaard J, Herlea V, Mauro FR, Dighiero G, Movsas B, Rassenti L, Kipps T, Baffa R, Fusco A, Mori M, Russo G, Liu CG, Neuberg D, Bullrich F, Negrini M, Croce CM. Familial cancer associated with a polymorphism in ARLTS1. N Engl J Med. 2005;352:1667–76.CrossRefPubMed
3.
go back to reference Yendamuri S, Trapasso F, Calin GA. ARLTS1 - a novel tumor suppressor gene. Cancer Lett. 2008;264:11–20.CrossRefPubMed Yendamuri S, Trapasso F, Calin GA. ARLTS1 - a novel tumor suppressor gene. Cancer Lett. 2008;264:11–20.CrossRefPubMed
4.
go back to reference Siltanen S, Wahlfors T, Schindler M, Saramaki OR, Mpindi JP, Latonen L, Vessella RL, Tammela TL, Kallioniemi O, Visakorpi T, Schleutker J. Contribution of ARLTS1 Cys148Arg (T442C) variant with prostate cancer risk and ARLTS1 function in prostate cancer cells. PLoS One. 2011;6:e26595.CrossRefPubMedPubMedCentral Siltanen S, Wahlfors T, Schindler M, Saramaki OR, Mpindi JP, Latonen L, Vessella RL, Tammela TL, Kallioniemi O, Visakorpi T, Schleutker J. Contribution of ARLTS1 Cys148Arg (T442C) variant with prostate cancer risk and ARLTS1 function in prostate cancer cells. PLoS One. 2011;6:e26595.CrossRefPubMedPubMedCentral
5.
go back to reference Petrocca F, Iliopoulos D, Qin HR, Nicoloso MS, Yendamuri S, Wojcik SE, Shimizu M, Di Leva G, Vecchione A, Trapasso F, Godwin AK, Negrini M, Calin GA, Croce CM. Alterations of the tumor suppressor gene ARLTS1 in ovarian cancer. Cancer Res. 2006;66:10287–91.CrossRefPubMed Petrocca F, Iliopoulos D, Qin HR, Nicoloso MS, Yendamuri S, Wojcik SE, Shimizu M, Di Leva G, Vecchione A, Trapasso F, Godwin AK, Negrini M, Calin GA, Croce CM. Alterations of the tumor suppressor gene ARLTS1 in ovarian cancer. Cancer Res. 2006;66:10287–91.CrossRefPubMed
6.
go back to reference Akisik E, Yazici H, Dalay N. ARLTS1, MDM2 and RAD51 gene variations are associated with familial breast cancer. Mol Biol Rep. 2011;38:343–8.CrossRefPubMed Akisik E, Yazici H, Dalay N. ARLTS1, MDM2 and RAD51 gene variations are associated with familial breast cancer. Mol Biol Rep. 2011;38:343–8.CrossRefPubMed
7.
go back to reference Masojc B, Mierzejewski M, Cybulski C, van de Wetering T, Debniak T, Gorski B, Jaworowska E, Tarnowska C, Lenner M, Scott RJ, Lubinski J. Cancer familial aggregation (CFA) and G446A polymorphism in ARLTS1 gene. Breast Cancer Res Treat. 2006;99:59–62.CrossRefPubMed Masojc B, Mierzejewski M, Cybulski C, van de Wetering T, Debniak T, Gorski B, Jaworowska E, Tarnowska C, Lenner M, Scott RJ, Lubinski J. Cancer familial aggregation (CFA) and G446A polymorphism in ARLTS1 gene. Breast Cancer Res Treat. 2006;99:59–62.CrossRefPubMed
8.
go back to reference Frank B, Hemminki K, Brenner H, Hoffmeister M, Chang-Claude J, Burwinkel B. ARLTS1 variants and risk of colorectal cancer. Cancer Lett. 2006;244:172–5.CrossRefPubMed Frank B, Hemminki K, Brenner H, Hoffmeister M, Chang-Claude J, Burwinkel B. ARLTS1 variants and risk of colorectal cancer. Cancer Lett. 2006;244:172–5.CrossRefPubMed
9.
go back to reference Xiao XY, Wang XD, Zang DY. MMP1-1607 1G/2G polymorphism and lung cancer risk: a meta-analysis. Tumour Biol. 2012;33:2385–92.CrossRefPubMed Xiao XY, Wang XD, Zang DY. MMP1-1607 1G/2G polymorphism and lung cancer risk: a meta-analysis. Tumour Biol. 2012;33:2385–92.CrossRefPubMed
10.
go back to reference Huang SX, Wu FX, Luo M, Ma L, Gao KF, Li J, Wu WJ, Huang S, Yang Q, Liu K, Zhao YN, Li LQ. The glutathione S-transferase P1 341C > T polymorphism and cancer risk: a meta-analysis of 28 case-control studies. PLoS One. 2013;8:e56722.CrossRefPubMedPubMedCentral Huang SX, Wu FX, Luo M, Ma L, Gao KF, Li J, Wu WJ, Huang S, Yang Q, Liu K, Zhao YN, Li LQ. The glutathione S-transferase P1 341C > T polymorphism and cancer risk: a meta-analysis of 28 case-control studies. PLoS One. 2013;8:e56722.CrossRefPubMedPubMedCentral
11.
go back to reference Salanti G, Amountza G, Ntzani EE, Ioannidis JP. Hardy-Weinberg equilibrium in genetic association studies: an empirical evaluation of reporting, deviations, and power. Eur J Hum Genet. 2005;13:840–8.CrossRefPubMed Salanti G, Amountza G, Ntzani EE, Ioannidis JP. Hardy-Weinberg equilibrium in genetic association studies: an empirical evaluation of reporting, deviations, and power. Eur J Hum Genet. 2005;13:840–8.CrossRefPubMed
12.
go back to reference Chen C, Li S, Lu X, Tan B, Huang C, Qin L. High resolution melting method to detect single nucleotide polymorphism of VKORC1 and CYP2C9. Int J Clin Exp Pathol. 2014;7:2558–64.PubMedPubMedCentral Chen C, Li S, Lu X, Tan B, Huang C, Qin L. High resolution melting method to detect single nucleotide polymorphism of VKORC1 and CYP2C9. Int J Clin Exp Pathol. 2014;7:2558–64.PubMedPubMedCentral
13.
go back to reference Czogalla KJ, Biswas A, Rost S, Watzka M, Oldenburg J. The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine-based ER retention motif. Blood. 2014;124:1354–62.CrossRefPubMed Czogalla KJ, Biswas A, Rost S, Watzka M, Oldenburg J. The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine-based ER retention motif. Blood. 2014;124:1354–62.CrossRefPubMed
14.
go back to reference Matagrin B, Montagut-Romans A, Damin M, Lemaire M, Popowycz F, Benoit E, Lattard V. Identification of VKORC1 genotype leading to resistance to tecarfarin. J Clin Pharmacol. 2014;54:896–900.CrossRefPubMed Matagrin B, Montagut-Romans A, Damin M, Lemaire M, Popowycz F, Benoit E, Lattard V. Identification of VKORC1 genotype leading to resistance to tecarfarin. J Clin Pharmacol. 2014;54:896–900.CrossRefPubMed
15.
go back to reference Kamal El-Din MA, Farhan MS, El Shiha RI, El-Kaffas RM, Mousa SM. Frequency of CYP2C9 and VKORC1 gene polymorphisms and their influence on warfarin dose in Egyptian pediatric patients. Paediatr Drugs. 2014;16:337–41.CrossRefPubMed Kamal El-Din MA, Farhan MS, El Shiha RI, El-Kaffas RM, Mousa SM. Frequency of CYP2C9 and VKORC1 gene polymorphisms and their influence on warfarin dose in Egyptian pediatric patients. Paediatr Drugs. 2014;16:337–41.CrossRefPubMed
16.
go back to reference Tomek A, Matoska V, Kolarova T, Neumann J, Sramek M, Sarbochova I, Taborsky L, Bojar M, Goetz P, Serebruany VL. The bleeding risk during warfarin therapy is associated with the number of variant alleles of CYP2C9 and VKORC1 genes. Cardiology. 2013;125:182–91.CrossRefPubMed Tomek A, Matoska V, Kolarova T, Neumann J, Sramek M, Sarbochova I, Taborsky L, Bojar M, Goetz P, Serebruany VL. The bleeding risk during warfarin therapy is associated with the number of variant alleles of CYP2C9 and VKORC1 genes. Cardiology. 2013;125:182–91.CrossRefPubMed
17.
go back to reference Shrif NE, Won HH, Lee ST, Park JH, Kim KK, Kim MJ, Kim S, Lee SY, Ki CS, Osman IM, Rhman EA, Ali IA, Idris MN, Kim JW. Evaluation of the effects of VKORC1 polymorphisms and haplotypes, CYP2C9 genotypes, and clinical factors on warfarin response in Sudanese patients. Eur J Clin Pharmacol. 2011;67:1119–30.CrossRefPubMed Shrif NE, Won HH, Lee ST, Park JH, Kim KK, Kim MJ, Kim S, Lee SY, Ki CS, Osman IM, Rhman EA, Ali IA, Idris MN, Kim JW. Evaluation of the effects of VKORC1 polymorphisms and haplotypes, CYP2C9 genotypes, and clinical factors on warfarin response in Sudanese patients. Eur J Clin Pharmacol. 2011;67:1119–30.CrossRefPubMed
18.
go back to reference Siltanen S, Syrjakoski K, Fagerholm R, Ikonen T, Lipman P, Mallott J, Holli K, Tammela TL, Jarvinen HJ, Mecklin JP, Aittomaki K, Blomqvist C, Bailey-Wilson JE, Nevanlinna H, Aaltonen LA, Schleutker J, Vahteristo P. ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer. Eur J Hum Genet. 2008;16:983–91.CrossRefPubMedPubMedCentral Siltanen S, Syrjakoski K, Fagerholm R, Ikonen T, Lipman P, Mallott J, Holli K, Tammela TL, Jarvinen HJ, Mecklin JP, Aittomaki K, Blomqvist C, Bailey-Wilson JE, Nevanlinna H, Aaltonen LA, Schleutker J, Vahteristo P. ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer. Eur J Hum Genet. 2008;16:983–91.CrossRefPubMedPubMedCentral
19.
go back to reference Yang XY, Yu H, Xi MR, Yang KX, Pan XL, Hu M, Peng ZL. Association of the ARLTS1 variants with familial ovarian cancer risk in China. Int J Gynecol Cancer. 2009;19:585–90.CrossRefPubMed Yang XY, Yu H, Xi MR, Yang KX, Pan XL, Hu M, Peng ZL. Association of the ARLTS1 variants with familial ovarian cancer risk in China. Int J Gynecol Cancer. 2009;19:585–90.CrossRefPubMed
20.
go back to reference Li X, Gast A, Rudnai P, Gurzau E, Koppova K, Hemminki K, Kumar R. ARLTS1 polymorphisms and basal cell carcinoma of the skin. Hereditary Cancer Clin Prac. 2007;5:25–9.CrossRef Li X, Gast A, Rudnai P, Gurzau E, Koppova K, Hemminki K, Kumar R. ARLTS1 polymorphisms and basal cell carcinoma of the skin. Hereditary Cancer Clin Prac. 2007;5:25–9.CrossRef
21.
go back to reference Castellvi-Bel S, Castells A, de Cid R, Munoz J, Balaguer F, Gonzalo V, Ruiz-Ponte C, Andreu M, Llor X, Jover R, Bessa X, Xicola RM, Pons E, Alenda C, Paya A, Carracedo A, Pique JM, Gastrointestinal Oncology Group of the Spanish Gastroenterological, A. Association of the ARLTS1 Cys148Arg variant with sporadic and familial colorectal cancer. Carcinogenesis. 2007;28:1687–91.CrossRefPubMed Castellvi-Bel S, Castells A, de Cid R, Munoz J, Balaguer F, Gonzalo V, Ruiz-Ponte C, Andreu M, Llor X, Jover R, Bessa X, Xicola RM, Pons E, Alenda C, Paya A, Carracedo A, Pique JM, Gastrointestinal Oncology Group of the Spanish Gastroenterological, A. Association of the ARLTS1 Cys148Arg variant with sporadic and familial colorectal cancer. Carcinogenesis. 2007;28:1687–91.CrossRefPubMed
22.
go back to reference Sellick GS, Catovsky D, Houlston RS. Relationship between ARLTS1 polymorphisms and risk of chronic lymphocytic leukemia. Leuk Res. 2006;30:1573–6.CrossRefPubMed Sellick GS, Catovsky D, Houlston RS. Relationship between ARLTS1 polymorphisms and risk of chronic lymphocytic leukemia. Leuk Res. 2006;30:1573–6.CrossRefPubMed
23.
go back to reference Frank B, Meyer P, Boettger MB, Hemminki K, Stapelmann H, Gast A, Schmitt C, Kumar R, Sergi C, Burwinkel B. ARLTS1 variants and melanoma risk. Int J Cancer. 2006;119:1736–7.CrossRefPubMed Frank B, Meyer P, Boettger MB, Hemminki K, Stapelmann H, Gast A, Schmitt C, Kumar R, Sergi C, Burwinkel B. ARLTS1 variants and melanoma risk. Int J Cancer. 2006;119:1736–7.CrossRefPubMed
24.
go back to reference Frank B, Hemminki K, Meindl A, Wappenschmidt B, Klaes R, Schmutzler RK, Untch M, Bugert P, Bartram CR, Burwinkel B. Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk. Int J Cancer. 2006;118:2505–8.CrossRefPubMed Frank B, Hemminki K, Meindl A, Wappenschmidt B, Klaes R, Schmutzler RK, Untch M, Bugert P, Bartram CR, Burwinkel B. Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk. Int J Cancer. 2006;118:2505–8.CrossRefPubMed
25.
go back to reference Siltanen S, Fischer D, Rantapero T, Laitinen V, Mpindi JP, Kallioniemi O, Wahlfors T, Schleutker J. ARLTS1 and prostate cancer risk--analysis of expression and regulation. PLoS One. 2013;8:e72040.CrossRefPubMedPubMedCentral Siltanen S, Fischer D, Rantapero T, Laitinen V, Mpindi JP, Kallioniemi O, Wahlfors T, Schleutker J. ARLTS1 and prostate cancer risk--analysis of expression and regulation. PLoS One. 2013;8:e72040.CrossRefPubMedPubMedCentral
26.
go back to reference Zambon CF, Pengo V, Padrini R, Basso D, Schiavon S, Fogar P, Nisi A, Frigo AC, Moz S, Pelloso M, Plebani M. VKORC1, CYP2C9 and CYP4F2 genetic-based algorithm for warfarin dosing: an Italian retrospective study. Pharmacogenomics. 2011;12:15–25.CrossRefPubMed Zambon CF, Pengo V, Padrini R, Basso D, Schiavon S, Fogar P, Nisi A, Frigo AC, Moz S, Pelloso M, Plebani M. VKORC1, CYP2C9 and CYP4F2 genetic-based algorithm for warfarin dosing: an Italian retrospective study. Pharmacogenomics. 2011;12:15–25.CrossRefPubMed
27.
go back to reference Ng D, Toure O, Fontaine L, McMaster ML, Goldin LR, Caporaso N, Toro JR. No association of ARLTS1 polymorphisms and risk for familial chronic lymphocytic leukaemia. Br J Haematol. 2007;137:173–5.CrossRefPubMed Ng D, Toure O, Fontaine L, McMaster ML, Goldin LR, Caporaso N, Toro JR. No association of ARLTS1 polymorphisms and risk for familial chronic lymphocytic leukaemia. Br J Haematol. 2007;137:173–5.CrossRefPubMed
28.
go back to reference De Brakeleer S, Teugels E, De Greve J. Familial cancer and ARLTS1. N Engl J Med. 2005;353:313–4. author reply 313-4.CrossRefPubMed De Brakeleer S, Teugels E, De Greve J. Familial cancer and ARLTS1. N Engl J Med. 2005;353:313–4. author reply 313-4.CrossRefPubMed
Metadata
Title
ARLTS1 polymorphism is associated with an increased risk of familial cancer: evidence from a meta-analysis
Authors
Yan Jiang
Chen-Yang Zhao
Li-Chun Cheng
Bing Xu
Hui-Yi Lv
Publication date
01-12-2017
Publisher
BioMed Central
Published in
Hereditary Cancer in Clinical Practice / Issue 1/2017
Electronic ISSN: 1897-4287
DOI
https://doi.org/10.1186/s13053-017-0068-7

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