Skip to main content
Top
Published in: NeuroMolecular Medicine 2/2014

01-06-2014 | Original Paper

Clinicopathologic Characteristics of Brain Tumors are Associated with the Presence and Patterns of TP53 Mutations: Evidence from the IARC TP53 Database

Author: Lyubov E. Salnikova

Published in: NeuroMolecular Medicine | Issue 2/2014

Login to get access

Abstract

Biological diversity in the development and progression of brain tumors may be based on the consequences of the nature of the TP53 mutation in the cancer sample. This study was designed to estimate the possible impact of the presence and spectrum of TP53 mutations on clinical variability of brain tumors using the IARC TP53 Database (R17). Somatic and germline mutation patterns differ in brain tumor carriers. The most frequent mutation in sporadic brain tumors is mutation R273C, which is relatively rare in grade 4 tumors compared with lower-grade tumors (p = 1.2 × 10−5, OR 0.43, 95 % CI 0.29–0.63). Mutations at all hot spots, DNA contact mutations, and mutations in the conserved regions of the TP53 gene are also more common in grade 1–3 tumors than in grade 4 tumors. The frequencies of missense mutations at hotspot codons and DNA contact mutations gradually decrease in all three age groups studied, indicating the role of these mutations in early-onset tumors. The role of TP53 somatic mutations in the development of brain tumors has been elucidated in the individual-participant meta-analysis that provided, for the first time, strong evidence that mean age at the onset of sporadic brain tumor is significantly lower in patients with mutated compared with wild-type TP53 in all groups stratified by tumor grade. The presence and patterns of TP53 mutations are associated mainly with the age at the onset and with the development of less malignant brain tumors. Malignant degeneration of brain tumors may depend on other genetic determinants.
Appendix
Available only for authorised users
Literature
go back to reference Batchelor, T. T., Betensky, R. A., Esposito, J. M., Pham, L. D., Dorfman, M. V., Piscatelli, N., et al. (2004). Age-dependent prognostic effects of genetic alterations in glioblastoma. Clinical Cancer Research, 10, 228–233.PubMedCrossRef Batchelor, T. T., Betensky, R. A., Esposito, J. M., Pham, L. D., Dorfman, M. V., Piscatelli, N., et al. (2004). Age-dependent prognostic effects of genetic alterations in glioblastoma. Clinical Cancer Research, 10, 228–233.PubMedCrossRef
go back to reference Bougeard, G., Sesboüé, R., Baert-Desurmont, S., Vasseur, S., Martin, C., Tinat, J., et al. (2008). Molecular basis of the Li–Fraumeni syndrome: An update from the French LFS families. Journal of Medical Genetics, 45, 535–538. doi:10.1136/jmg.2008.057570.PubMedCrossRef Bougeard, G., Sesboüé, R., Baert-Desurmont, S., Vasseur, S., Martin, C., Tinat, J., et al. (2008). Molecular basis of the Li–Fraumeni syndrome: An update from the French LFS families. Journal of Medical Genetics, 45, 535–538. doi:10.​1136/​jmg.​2008.​057570.PubMedCrossRef
go back to reference Chen, P., Aldape, K., Wiencke, J. K., Kelsey, K. T., Miike, R., Davis, R. L., et al. (2001). Ethnicity delineates different genetic pathways in malignant glioma. Cancer Research, 61, 3949–3954.PubMed Chen, P., Aldape, K., Wiencke, J. K., Kelsey, K. T., Miike, R., Davis, R. L., et al. (2001). Ethnicity delineates different genetic pathways in malignant glioma. Cancer Research, 61, 3949–3954.PubMed
go back to reference Chen, Y. J., Hakin-Smith, V., Teo, M., Xinarianos, G. E., Jellinek, D. A., Carroll, T., et al. (2006). Association of mutant TP53 with alternative lengthening of telomeres and favorable prognosis in glioma. Cancer Research, 66, 6473–6476. doi:10.1158/0008-5472.CAN-06-0910.PubMedCrossRef Chen, Y. J., Hakin-Smith, V., Teo, M., Xinarianos, G. E., Jellinek, D. A., Carroll, T., et al. (2006). Association of mutant TP53 with alternative lengthening of telomeres and favorable prognosis in glioma. Cancer Research, 66, 6473–6476. doi:10.​1158/​0008-5472.​CAN-06-0910.PubMedCrossRef
go back to reference Dearth, L. R., Qian, H., Wang, T., Baroni, T. E., Zeng, J., Chen, S. W., et al. (2007). Inactive full-length p53 mutants lacking dominant wild-type p53 inhibition highlight loss of heterozygosity as an important aspect of p53 status in human cancers. Carcinogenesis, 28, 289–298. doi:10.1093/carcin/bgl132.PubMedCrossRef Dearth, L. R., Qian, H., Wang, T., Baroni, T. E., Zeng, J., Chen, S. W., et al. (2007). Inactive full-length p53 mutants lacking dominant wild-type p53 inhibition highlight loss of heterozygosity as an important aspect of p53 status in human cancers. Carcinogenesis, 28, 289–298. doi:10.​1093/​carcin/​bgl132.PubMedCrossRef
go back to reference Felsberg, J., Rapp, M., Loeser, S., Fimmers, R., Stummer, W., Goeppert, M., et al. (2009). Prognostic significance of molecular markers and extent of resection in primary glioblastoma patients. Clinical Cancer Research, 15, 6683–6693. doi:10.1158/1078-0432.CCR-08-2801.PubMedCrossRef Felsberg, J., Rapp, M., Loeser, S., Fimmers, R., Stummer, W., Goeppert, M., et al. (2009). Prognostic significance of molecular markers and extent of resection in primary glioblastoma patients. Clinical Cancer Research, 15, 6683–6693. doi:10.​1158/​1078-0432.​CCR-08-2801.PubMedCrossRef
go back to reference Fernández-Cuesta, L., Oakman, C., Falagan-Lotsch, P., Smoth, K. S., Quinaux, E., Buyse, M., et al. (2012). Prognostic and predictive value of TP53 mutations in node-positive breast cancer patients treated with anthracycline- or anthracycline/taxane-based adjuvant therapy: Results from the BIG 02-98 phase III trial. Breast Cancer Research, 14(3), R70. doi:10.1186/bcr3179.PubMedCentralPubMedCrossRef Fernández-Cuesta, L., Oakman, C., Falagan-Lotsch, P., Smoth, K. S., Quinaux, E., Buyse, M., et al. (2012). Prognostic and predictive value of TP53 mutations in node-positive breast cancer patients treated with anthracycline- or anthracycline/taxane-based adjuvant therapy: Results from the BIG 02-98 phase III trial. Breast Cancer Research, 14(3), R70. doi:10.​1186/​bcr3179.PubMedCentralPubMedCrossRef
go back to reference Forrester, K., Lupold, S. E., Ott, V. L., Chay, C. H., Band, V., Wang, X. W., et al. (1995). Effects of p53 mutants on wild-type p53-mediated transactivation are cell type dependent. Oncogene, 10, 2103–2111.PubMed Forrester, K., Lupold, S. E., Ott, V. L., Chay, C. H., Band, V., Wang, X. W., et al. (1995). Effects of p53 mutants on wild-type p53-mediated transactivation are cell type dependent. Oncogene, 10, 2103–2111.PubMed
go back to reference Hainaut, P., Olivier, M., & Wiman, K. (Eds.). (2013). p53 in the clinics. New York: Springer. Hainaut, P., Olivier, M., & Wiman, K. (Eds.). (2013). p53 in the clinics. New York: Springer.
go back to reference Ishii, N., Tada, M., Hamou, M. F., Janzer, R. C., Meagher-Villemure, K., Wiestler, O. D., et al. (1999). Cells with TP53 mutations in low grade astrocytic tumors evolve clonally to malignancy and are an unfavorable prognostic factor. Oncogene, 18, 5870–5878.PubMedCrossRef Ishii, N., Tada, M., Hamou, M. F., Janzer, R. C., Meagher-Villemure, K., Wiestler, O. D., et al. (1999). Cells with TP53 mutations in low grade astrocytic tumors evolve clonally to malignancy and are an unfavorable prognostic factor. Oncogene, 18, 5870–5878.PubMedCrossRef
go back to reference Jha, P., Suri, V., Singh, G., Jha, P., Purkait, S., Pathak, P., et al. (2011). Characterization of molecular genetic alterations in GBMs highlights a distinctive molecular profile in young adults. Diagnostic Molecular Pathology, 20, 225–232. doi:10.1097/PDM.0b013e31821c30bc.PubMedCrossRef Jha, P., Suri, V., Singh, G., Jha, P., Purkait, S., Pathak, P., et al. (2011). Characterization of molecular genetic alterations in GBMs highlights a distinctive molecular profile in young adults. Diagnostic Molecular Pathology, 20, 225–232. doi:10.​1097/​PDM.​0b013e31821c30bc​.PubMedCrossRef
go back to reference Kato, S., Han, S. Y., Liu, W., Otsuka, K., Shibata, H., Kanamaru, R., et al. (2003). Understanding the function–structure and function–mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis. Proceedings of the National Academy of Sciences of the United States of America, 100, 8424–8429. doi:10.1073/pnas.1431692100.PubMedCentralPubMedCrossRef Kato, S., Han, S. Y., Liu, W., Otsuka, K., Shibata, H., Kanamaru, R., et al. (2003). Understanding the function–structure and function–mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis. Proceedings of the National Academy of Sciences of the United States of America, 100, 8424–8429. doi:10.​1073/​pnas.​1431692100.PubMedCentralPubMedCrossRef
go back to reference Köbel, M., Kalloger, S. E., Boyd, N., McKinney, S., Mehl, E., Palmer, C., et al. (2008). Ovarian carcinoma subtypes are different diseases: Implications for biomarker studies. PLoS Med, 5(12), e232. 10.1371/journal.pmed.0050232.PubMedCentralPubMedCrossRef Köbel, M., Kalloger, S. E., Boyd, N., McKinney, S., Mehl, E., Palmer, C., et al. (2008). Ovarian carcinoma subtypes are different diseases: Implications for biomarker studies. PLoS Med, 5(12), e232. 10.1371/journal.pmed.0050232.PubMedCentralPubMedCrossRef
go back to reference Kösel, S., Scheithauer, B. W., & Graeber, M. B. (2001). Genotype-phenotype correlation in gemistocytic astrocytomas. Neurosurgery, 48, 187–193.PubMedCrossRef Kösel, S., Scheithauer, B. W., & Graeber, M. B. (2001). Genotype-phenotype correlation in gemistocytic astrocytomas. Neurosurgery, 48, 187–193.PubMedCrossRef
go back to reference Kraus, J. A., Wenghoefer, M., Glesmann, N., Mohr, S., Beck, M., Schmidt, M. C., et al. (2001). TP53 gene mutations, nuclear p53 accumulation, expression of Waf/p21, Bcl-2, and CD95 (APO-1/Fas) proteins are not prognostic factors in de novo glioblastoma multiforme. Journal of Neuro-oncology, 52, 263–272.PubMedCrossRef Kraus, J. A., Wenghoefer, M., Glesmann, N., Mohr, S., Beck, M., Schmidt, M. C., et al. (2001). TP53 gene mutations, nuclear p53 accumulation, expression of Waf/p21, Bcl-2, and CD95 (APO-1/Fas) proteins are not prognostic factors in de novo glioblastoma multiforme. Journal of Neuro-oncology, 52, 263–272.PubMedCrossRef
go back to reference Louis, D. N., von Deimling, A., Chung, R. Y., Rubio, M. P., Whaley, J. M., Eibl, R. H., et al. (1993). Comparative study of p53 gene and protein alterations in human astrocytic tumors. Journal of Neuropathology and Experimental Neurology, 52, 31–38.PubMedCrossRef Louis, D. N., von Deimling, A., Chung, R. Y., Rubio, M. P., Whaley, J. M., Eibl, R. H., et al. (1993). Comparative study of p53 gene and protein alterations in human astrocytic tumors. Journal of Neuropathology and Experimental Neurology, 52, 31–38.PubMedCrossRef
go back to reference McLendon, R. E., Herndon, J. E., I. I., West, B., Reardon, D., Wiltshire, R., Rasheed, B. K., et al. (2005). Survival analysis of presumptive prognostic markers among oligodendrogliomas. Cancer, 104, 1693–1699. doi:10.1002/cncr.21362.PubMedCrossRef McLendon, R. E., Herndon, J. E., I. I., West, B., Reardon, D., Wiltshire, R., Rasheed, B. K., et al. (2005). Survival analysis of presumptive prognostic markers among oligodendrogliomas. Cancer, 104, 1693–1699. doi:10.​1002/​cncr.​21362.PubMedCrossRef
go back to reference Mitchell, G., Ballinger, M. L., Wong, S., Hewitt, C., James, P., Young, M. A., et al. (2013). High frequency of germline TP53 mutations in a prospective adult-onset sarcoma cohort. PLoS ONE, 8(7), e69026. 10.1371/journal.pone.0069026.PubMedCentralPubMedCrossRef Mitchell, G., Ballinger, M. L., Wong, S., Hewitt, C., James, P., Young, M. A., et al. (2013). High frequency of germline TP53 mutations in a prospective adult-onset sarcoma cohort. PLoS ONE, 8(7), e69026. 10.1371/journal.pone.0069026.PubMedCentralPubMedCrossRef
go back to reference Mukhopadhyay, T., & Roth, J. A. (1993). A codon 248 p53 mutation retains tumor suppressor function as shown by enhancement of tumor growth by antisense p53. Cancer Research, 53, 4362–4366.PubMed Mukhopadhyay, T., & Roth, J. A. (1993). A codon 248 p53 mutation retains tumor suppressor function as shown by enhancement of tumor growth by antisense p53. Cancer Research, 53, 4362–4366.PubMed
go back to reference Olivier, M. (2013). TP53 somatic mutations: Prognostic and predictive value in human cancers. In P. Hainaut, M. Olivier, & K. G. Wiman (Eds.), p53 in the clinics (pp. 127–146). New York: Springer.CrossRef Olivier, M. (2013). TP53 somatic mutations: Prognostic and predictive value in human cancers. In P. Hainaut, M. Olivier, & K. G. Wiman (Eds.), p53 in the clinics (pp. 127–146). New York: Springer.CrossRef
go back to reference Olivier, M., Eeles, R., Hollstein, M., Khan, M. A., Harris, C. C., & Hainaut, P. (2002). The IARC TP53 Database: New online mutation analysis and recommendations to users. Human Mutation, 19, 607–614. doi:10.1002/humu.10081.PubMedCrossRef Olivier, M., Eeles, R., Hollstein, M., Khan, M. A., Harris, C. C., & Hainaut, P. (2002). The IARC TP53 Database: New online mutation analysis and recommendations to users. Human Mutation, 19, 607–614. doi:10.​1002/​humu.​10081.PubMedCrossRef
go back to reference Olivier, M., Goldgar, D. E., Sodha, N., Ohgaki, H., Kleihues, P., Hainaut, P., et al. (2003). Li-Fraumeni and related syndromes: Correlation between tumor type, family structure, and TP53 genotype. Cancer Research, 63, 6643–6650.PubMed Olivier, M., Goldgar, D. E., Sodha, N., Ohgaki, H., Kleihues, P., Hainaut, P., et al. (2003). Li-Fraumeni and related syndromes: Correlation between tumor type, family structure, and TP53 genotype. Cancer Research, 63, 6643–6650.PubMed
go back to reference Olivier, M., Petitjean, A., Marcel, V., Pétré, A., Mounawar, M., Plymoth, A., et al. (2009). Recent advances in p53 research: An interdisciplinary perspective. Cancer Gene Therapy, 16, 1–12. doi:10.1038/cgt.2008.69.PubMedCrossRef Olivier, M., Petitjean, A., Marcel, V., Pétré, A., Mounawar, M., Plymoth, A., et al. (2009). Recent advances in p53 research: An interdisciplinary perspective. Cancer Gene Therapy, 16, 1–12. doi:10.​1038/​cgt.​2008.​69.PubMedCrossRef
go back to reference O’Shea, D., O’Riain, C., Taylor, C., Waters, R., Carlotti, E., Macdougall, F., et al. (2008). The presence of TP53 mutation at diagnosis of follicular lymphoma identifies a high-risk group of patients with shortened time to disease progression and poorer overall survival. Blood, 112, 3126–3129. doi:10.1182/blood-2008-05-154013.PubMedCentralPubMedCrossRef O’Shea, D., O’Riain, C., Taylor, C., Waters, R., Carlotti, E., Macdougall, F., et al. (2008). The presence of TP53 mutation at diagnosis of follicular lymphoma identifies a high-risk group of patients with shortened time to disease progression and poorer overall survival. Blood, 112, 3126–3129. doi:10.​1182/​blood-2008-05-154013.PubMedCentralPubMedCrossRef
go back to reference Peraud, A., Kreth, F. W., Wiestler, O. D., Kleihues, P., & Reulen, H. J. (2002). Prognostic impact of TP53 mutations and P53 protein overexpression in supratentorial WHO grade II astrocytomas and oligoastrocytomas. Clinical Cancer Research, 8, 1117–1124.PubMed Peraud, A., Kreth, F. W., Wiestler, O. D., Kleihues, P., & Reulen, H. J. (2002). Prognostic impact of TP53 mutations and P53 protein overexpression in supratentorial WHO grade II astrocytomas and oligoastrocytomas. Clinical Cancer Research, 8, 1117–1124.PubMed
go back to reference Petitjean, A., Achatz, M. I., Borresen-Dale, A. L., Hainaut, P., & Olivier, M. (2007a). P53 mutations in human cancers: functional selection and impact on cancer prognosis and outcomes. Oncogene, 26, 2157–2165. 10.1038/sj.onc.1210302.PubMedCrossRef Petitjean, A., Achatz, M. I., Borresen-Dale, A. L., Hainaut, P., & Olivier, M. (2007a). P53 mutations in human cancers: functional selection and impact on cancer prognosis and outcomes. Oncogene, 26, 2157–2165. 10.1038/sj.onc.1210302.PubMedCrossRef
go back to reference Petitjean, A., Mathe, E., Kato, S., Ishioka, C., Tavtigian, S. V., Hainaut, P., et al. (2007b). Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: Lessons from recent developments in the IARC TP53 Database. Human Mutation, 28, 622–629. doi:10.1002/humu.20495.PubMedCrossRef Petitjean, A., Mathe, E., Kato, S., Ishioka, C., Tavtigian, S. V., Hainaut, P., et al. (2007b). Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: Lessons from recent developments in the IARC TP53 Database. Human Mutation, 28, 622–629. doi:10.​1002/​humu.​20495.PubMedCrossRef
go back to reference Pollack, I. F., Finkelstein, S. D., Woods, J., Burnham, J., Holmes, E. J., Hamilton, R. L., et al. (2002). Expression of p53 and prognosis in children with malignant gliomas. New England Journal of Medicine, 346, 420–427. doi:10.1056/NEJMoa012224.PubMedCrossRef Pollack, I. F., Finkelstein, S. D., Woods, J., Burnham, J., Holmes, E. J., Hamilton, R. L., et al. (2002). Expression of p53 and prognosis in children with malignant gliomas. New England Journal of Medicine, 346, 420–427. doi:10.​1056/​NEJMoa012224.PubMedCrossRef
go back to reference Powell, B., Soong, R., Iacopetta, B., Seshadri, R., & Smith, D. R. (2000). Prognostic significance of mutations to different structural and functional regions of the p53 gene in breast cancer. Clinical Cancer Research, 6, 443–451.PubMed Powell, B., Soong, R., Iacopetta, B., Seshadri, R., & Smith, D. R. (2000). Prognostic significance of mutations to different structural and functional regions of the p53 gene in breast cancer. Clinical Cancer Research, 6, 443–451.PubMed
go back to reference Rasheed, B. K., McLendon, R. E., Herndon, J. E., Friedman, H. S., Friedman, A. H., Bigner, D. D., et al. (1994). Alterations of the TP53 gene in human gliomas. Cancer Research, 54, 1324–1330.PubMed Rasheed, B. K., McLendon, R. E., Herndon, J. E., Friedman, H. S., Friedman, A. H., Bigner, D. D., et al. (1994). Alterations of the TP53 gene in human gliomas. Cancer Research, 54, 1324–1330.PubMed
go back to reference Reifenberger, J., Ring, G. U., Gies, U., Cobbers, L., Oberstrass, J., An, H. X., et al. (1996). Analysis of p53 mutation and epidermal growth factor receptor amplification in recurrent gliomas with malignant progression. Journal of Neuropathology and Experimental Neurology, 55, 822–831.PubMedCrossRef Reifenberger, J., Ring, G. U., Gies, U., Cobbers, L., Oberstrass, J., An, H. X., et al. (1996). Analysis of p53 mutation and epidermal growth factor receptor amplification in recurrent gliomas with malignant progression. Journal of Neuropathology and Experimental Neurology, 55, 822–831.PubMedCrossRef
go back to reference Rücker, F. G., Schlenk, R. F., Bullinger, L., Kayser, S., Teleanu, V., Kett, H., et al. (2012). TP53 alterations in acute myeloid leukemia with complex karyotype correlate with specific copy number alterations, monosomal karyotype, and dismal outcome. Blood, 119, 2114–2121. doi:10.1182/blood-2011-08-375758.PubMedCrossRef Rücker, F. G., Schlenk, R. F., Bullinger, L., Kayser, S., Teleanu, V., Kett, H., et al. (2012). TP53 alterations in acute myeloid leukemia with complex karyotype correlate with specific copy number alterations, monosomal karyotype, and dismal outcome. Blood, 119, 2114–2121. doi:10.​1182/​blood-2011-08-375758.PubMedCrossRef
go back to reference Schmidt, M. C., Antweiler, S., Urban, N., Mueller, W., Kuklik, A., Meyer-Puttlitz, B., et al. (2002). Impact of genotype and morphology on the prognosis of glioblastoma. Journal of Neuropathology and Experimental Neurology, 61, 321–328.PubMed Schmidt, M. C., Antweiler, S., Urban, N., Mueller, W., Kuklik, A., Meyer-Puttlitz, B., et al. (2002). Impact of genotype and morphology on the prognosis of glioblastoma. Journal of Neuropathology and Experimental Neurology, 61, 321–328.PubMed
go back to reference Smith, J. S., Tachibana, I., Passe, S. M., Huntley, B. K., Borell, T. J., Iturria, N., et al. (2001). PTEN mutation, EGFR amplification, and outcome in patients with anaplastic astrocytoma and glioblastoma multiforme. Journal of the National Cancer Institute, 93, 1246–1256. doi:10.1093/jnci/93.16.1246.PubMedCrossRef Smith, J. S., Tachibana, I., Passe, S. M., Huntley, B. K., Borell, T. J., Iturria, N., et al. (2001). PTEN mutation, EGFR amplification, and outcome in patients with anaplastic astrocytoma and glioblastoma multiforme. Journal of the National Cancer Institute, 93, 1246–1256. doi:10.​1093/​jnci/​93.​16.​1246.PubMedCrossRef
go back to reference Stander, M., Peraud, A., Leroch, B., & Kreth, F. W. (2004). Prognostic impact of TP53 mutation status for adult patients with supratentorial World Health Organization Grade II astrocytoma or oligoastrocytoma: A longterm analysis. Cancer, 101, 1028–1035. doi:10.1002/cncr.20432.PubMedCrossRef Stander, M., Peraud, A., Leroch, B., & Kreth, F. W. (2004). Prognostic impact of TP53 mutation status for adult patients with supratentorial World Health Organization Grade II astrocytoma or oligoastrocytoma: A longterm analysis. Cancer, 101, 1028–1035. doi:10.​1002/​cncr.​20432.PubMedCrossRef
go back to reference Surveillance, Epidemiology, and End Results (SEER) Program (www.seer.cancer.gov) SEER*Stat Database: Incidence—SEER 18 Regs Research Data + Hurricane Katrina Impacted Louisiana Cases, Nov 2012 Sub (1973-2010 varying)—Linked To County Attributes—Total U.S., 1969-2011 Counties, National Cancer Institute, DCCPS, Surveillance Research Program, Surveillance Systems Branch, released April 2013, based on the November 2012 submission. Surveillance, Epidemiology, and End Results (SEER) Program (www.​seer.​cancer.​gov) SEER*Stat Database: Incidence—SEER 18 Regs Research Data + Hurricane Katrina Impacted Louisiana Cases, Nov 2012 Sub (1973-2010 varying)—Linked To County Attributes—Total U.S., 1969-2011 Counties, National Cancer Institute, DCCPS, Surveillance Research Program, Surveillance Systems Branch, released April 2013, based on the November 2012 submission.
go back to reference Thon, N., Eigenbrod, S., Kreth, S., Lutz, J., Tonn, J. C., Kretzschmar, H., et al. (2012). IDH1 mutations in grade II astrocytomas are associated with unfavorable progression-free survival and prolonged postrecurrence survival. Cancer, 118, 452–460. doi:10.1002/cncr.26298.PubMedCrossRef Thon, N., Eigenbrod, S., Kreth, S., Lutz, J., Tonn, J. C., Kretzschmar, H., et al. (2012). IDH1 mutations in grade II astrocytomas are associated with unfavorable progression-free survival and prolonged postrecurrence survival. Cancer, 118, 452–460. doi:10.​1002/​cncr.​26298.PubMedCrossRef
go back to reference Vaupel, P. (2010). Metabolic microenvironment of tumor cells: A key factor in malignant progression. Experimental Oncology, 32, 125–127.PubMed Vaupel, P. (2010). Metabolic microenvironment of tumor cells: A key factor in malignant progression. Experimental Oncology, 32, 125–127.PubMed
go back to reference Walker, C., du Plessis, D. G., Joyce, K. A., Fildes, D., Gee, A., Haylock, B., et al. (2005). Molecular pathology and clinical characteristics of oligodendroglial neoplasms. Annals of Neurology, 57, 855–865. doi:10.1002/ana.20496.PubMedCrossRef Walker, C., du Plessis, D. G., Joyce, K. A., Fildes, D., Gee, A., Haylock, B., et al. (2005). Molecular pathology and clinical characteristics of oligodendroglial neoplasms. Annals of Neurology, 57, 855–865. doi:10.​1002/​ana.​20496.PubMedCrossRef
go back to reference Watanabe, T., Katayama, Y., Yoshino, A., Komine, C., & Yokoyama, T. (2003). Deregulation of the TP53/p14ARF tumor suppressor pathway in low-grade diffuse astrocytomas and its influence on clinical course. Clinical Cancer Research, 9, 4884–4890.PubMed Watanabe, T., Katayama, Y., Yoshino, A., Komine, C., & Yokoyama, T. (2003). Deregulation of the TP53/p14ARF tumor suppressor pathway in low-grade diffuse astrocytomas and its influence on clinical course. Clinical Cancer Research, 9, 4884–4890.PubMed
go back to reference Wiestler, B., Claus, R., Hartlieb, S. A., Schliesser, M. G., Weiss, E. K., Hielscher, T., et al. (2013). Malignant astrocytomas of elderly patients lack favorable molecular markers: An analysis of the NOA-08 study collective. Neuro-oncology, 15, 1017–1026. doi:10.1093/neuonc/not043.PubMedCrossRef Wiestler, B., Claus, R., Hartlieb, S. A., Schliesser, M. G., Weiss, E. K., Hielscher, T., et al. (2013). Malignant astrocytomas of elderly patients lack favorable molecular markers: An analysis of the NOA-08 study collective. Neuro-oncology, 15, 1017–1026. doi:10.​1093/​neuonc/​not043.PubMedCrossRef
go back to reference Wunder, J. S., Gokgoz, N., Parkes, R., Bull, S. B., Eskandarian, S., & Davis, A. M. (2005). TP53 mutations and outcome in osteosarcoma: A prospective, multicenter study. Journal of Clinical Oncology, 23, 1483–1490. doi:10.1200/JCO.2005.04.074.PubMedCrossRef Wunder, J. S., Gokgoz, N., Parkes, R., Bull, S. B., Eskandarian, S., & Davis, A. M. (2005). TP53 mutations and outcome in osteosarcoma: A prospective, multicenter study. Journal of Clinical Oncology, 23, 1483–1490. doi:10.​1200/​JCO.​2005.​04.​074.PubMedCrossRef
go back to reference Zerdoumi, Y., Aury-Landas, J., Bonaïti-Pellié, C., Derambure, C., Sesboüé, R., & Renaux-Petel, M. (2013). Drastic effect of germline TP53 missense mutations in Li–Fraumeni patients. Human Mutation, 34, 453–461. doi:10.1002/humu.22254.PubMedCrossRef Zerdoumi, Y., Aury-Landas, J., Bonaïti-Pellié, C., Derambure, C., Sesboüé, R., & Renaux-Petel, M. (2013). Drastic effect of germline TP53 missense mutations in Li–Fraumeni patients. Human Mutation, 34, 453–461. doi:10.​1002/​humu.​22254.PubMedCrossRef
Metadata
Title
Clinicopathologic Characteristics of Brain Tumors are Associated with the Presence and Patterns of TP53 Mutations: Evidence from the IARC TP53 Database
Author
Lyubov E. Salnikova
Publication date
01-06-2014
Publisher
Springer US
Published in
NeuroMolecular Medicine / Issue 2/2014
Print ISSN: 1535-1084
Electronic ISSN: 1559-1174
DOI
https://doi.org/10.1007/s12017-014-8290-1

Other articles of this Issue 2/2014

NeuroMolecular Medicine 2/2014 Go to the issue