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Erschienen in: Tumor Biology 1/2014

01.01.2014 | Research Article

DNA polymerase β mutations and survival of patients with esophageal squamous cell carcinoma in Linzhou City, China

verfasst von: Min Li, Wenqiao Zang, Yuanyuan Wang, Yunyun Ma, Xiaoyan Xuan, Jimin Zhao, Lulu Liu, Ziming Dong, Guoqiang Zhao

Erschienen in: Tumor Biology | Ausgabe 1/2014

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Abstract

Linzhou City in northern China has a high incidence of esophageal squamous cell carcinoma (ESCC). This study retrospectively analyzed the data of 231 cases with ESCC collected from 1998 to 2012. Mutations of DNA polymerase β (polβ) gene in the ESCC samples from patients in Linzhou City were examined by amplifying polβ cDNA by RT-PCR followed by cloning and sequencing. Mutations in polβ were found in 105 cases (45.9 %). Nine types of mutations were identified in the polβ cDNA; the most common were 177–234 nt deletion (11.3 %), 462 nt G → T (9.1 %), and 648 nt G → C (6.9 %). Mutations in polβ appeared to be associated with TNM status (P = 0.048). Follow-up data was used for survival analysis. The overall 5-year survival rate of the 231 patients was 37.4 %; the rate for patients with wild-type (WT) polβ was 41.8 %. Compared with the WT polβ group, the median survival for patients with specific mutations (177–234 nt deletion, 462 nt G → T, or 613 nt A → T) was significantly shorter (all P = 0.000), and the 5-year survival rate decreased to 0 %. Patients with the 648 nt G → C mutation had improved survival (P = 0.000) with a 5-year survival rate of 100 %. Our results identified nine types of mutations within polβ cDNA in ESCC patients with four mutations related to patient survival.
Literatur
1.
2.
Zurück zum Zitat Parkin DM, Pisani P, Ferlay J. Estimates of the worldwide incidence of 25 major cancers in 1990. Int J Cancer. 1999;80(6):827–41.PubMedCrossRef Parkin DM, Pisani P, Ferlay J. Estimates of the worldwide incidence of 25 major cancers in 1990. Int J Cancer. 1999;80(6):827–41.PubMedCrossRef
3.
Zurück zum Zitat Genetic alterations in esophageal cancer and their relevance to etiology and pathogenesis: a review. Int J Cancer. 1996;69(3):225–35. Genetic alterations in esophageal cancer and their relevance to etiology and pathogenesis: a review. Int J Cancer. 1996;69(3):225–35.
4.
Zurück zum Zitat Idriss HT, Al-Assar O, Wilson SH. DNA polymerase beta. Int J Biochem Cell Biol. 2002;34(4):321–4.PubMedCrossRef Idriss HT, Al-Assar O, Wilson SH. DNA polymerase beta. Int J Biochem Cell Biol. 2002;34(4):321–4.PubMedCrossRef
5.
Zurück zum Zitat Bergoglio V, Pillaire MJ, Lacroix-Triki M, Raynaud-Messina B, Canitrot Y, Bieth A, et al. Deregulated DNA polymerase beta induces chromosome instability and tumorigenesis. Cancer Res. 2002;62(12):3511–4.PubMed Bergoglio V, Pillaire MJ, Lacroix-Triki M, Raynaud-Messina B, Canitrot Y, Bieth A, et al. Deregulated DNA polymerase beta induces chromosome instability and tumorigenesis. Cancer Res. 2002;62(12):3511–4.PubMed
6.
Zurück zum Zitat Canitrot Y, Frechet M, Servant L, Cazaux C, Hoffmann JS. Overexpression of DNA polymerase beta: a genomic instability enhancer process. FASEB J. 1999;13(9):1107–11.PubMed Canitrot Y, Frechet M, Servant L, Cazaux C, Hoffmann JS. Overexpression of DNA polymerase beta: a genomic instability enhancer process. FASEB J. 1999;13(9):1107–11.PubMed
7.
Zurück zum Zitat Canitrot Y, Cazaux C, Fréchet M, Bouayadi K, Lesca C, Salles B, et al. Overexpression of DNA polymerase beta in cell results in a mutator phenotype and a decreased sensitivity to anticancer drugs. Proc Natl Acad Sci U S A. 1998;95(21):12586–90.PubMedCentralPubMedCrossRef Canitrot Y, Cazaux C, Fréchet M, Bouayadi K, Lesca C, Salles B, et al. Overexpression of DNA polymerase beta in cell results in a mutator phenotype and a decreased sensitivity to anticancer drugs. Proc Natl Acad Sci U S A. 1998;95(21):12586–90.PubMedCentralPubMedCrossRef
8.
Zurück zum Zitat Sliwinski T, Ziemba P, Morawiec Z, Kowalski M, Zadrozny M, Blasiak J. Polymorphisms of the DNA polymerase beta gene in breast cancer. Breast Cancer Res Treat. 2007;103(2):161–6.PubMedCrossRef Sliwinski T, Ziemba P, Morawiec Z, Kowalski M, Zadrozny M, Blasiak J. Polymorphisms of the DNA polymerase beta gene in breast cancer. Breast Cancer Res Treat. 2007;103(2):161–6.PubMedCrossRef
9.
Zurück zum Zitat Lang T, Dalal S, Chikova A, DiMaio D, Sweasy JB. The E295K DNA polymerase beta gastric cancer-associated variant interferes with base excision repair and induces cellular transformation. Mol Cell Biol. 2007;27(15):5587–96.PubMedCentralPubMedCrossRef Lang T, Dalal S, Chikova A, DiMaio D, Sweasy JB. The E295K DNA polymerase beta gastric cancer-associated variant interferes with base excision repair and induces cellular transformation. Mol Cell Biol. 2007;27(15):5587–96.PubMedCentralPubMedCrossRef
10.
Zurück zum Zitat Tan XH, Zhao M, Pan KF, Dong Y, Dong B, Feng GJ, et al. Frequent mutation related with overexpression of DNA polymerase beta in primary tumors and precancerous lesions of human stomach. Cancer Lett. 2005;220(1):101–14.PubMedCrossRef Tan XH, Zhao M, Pan KF, Dong Y, Dong B, Feng GJ, et al. Frequent mutation related with overexpression of DNA polymerase beta in primary tumors and precancerous lesions of human stomach. Cancer Lett. 2005;220(1):101–14.PubMedCrossRef
11.
Zurück zum Zitat Eydmann ME, Knowles MA. Mutation analysis of 8p genes POLB and PPP2CB in bladder cancer. Cancer Genet Cytogenet. 1997;93(2):167–71.PubMedCrossRef Eydmann ME, Knowles MA. Mutation analysis of 8p genes POLB and PPP2CB in bladder cancer. Cancer Genet Cytogenet. 1997;93(2):167–71.PubMedCrossRef
12.
Zurück zum Zitat Dalal S, Hile S, Eckert KA, Sun KW, Starcevic D, Sweasy JB. Prostate-cancer-associated I260M variant of DNA polymerase beta is a sequence-specific mutator. Biochemistry. 2005;44(48):15664–73.PubMedCrossRef Dalal S, Hile S, Eckert KA, Sun KW, Starcevic D, Sweasy JB. Prostate-cancer-associated I260M variant of DNA polymerase beta is a sequence-specific mutator. Biochemistry. 2005;44(48):15664–73.PubMedCrossRef
13.
Zurück zum Zitat Albertella MR, Lau A, O’Connor MJ. The overexpression of specialized DNA polymerases in cancer. DNA Repair (Amst). 2005;4(5):583–93.CrossRef Albertella MR, Lau A, O’Connor MJ. The overexpression of specialized DNA polymerases in cancer. DNA Repair (Amst). 2005;4(5):583–93.CrossRef
14.
Zurück zum Zitat Sobol RW, Foley JF, Nyska A, Davidson MG, Wilson SH. Regulated over-expression of DNA polymerase beta mediates early onset cataract in mice. DNA Repair (Amst). 2003;2(5):609–22.CrossRef Sobol RW, Foley JF, Nyska A, Davidson MG, Wilson SH. Regulated over-expression of DNA polymerase beta mediates early onset cataract in mice. DNA Repair (Amst). 2003;2(5):609–22.CrossRef
15.
Zurück zum Zitat Khanra K, Panda K, Bhattacharya C, Mitra AK, Sarkar R, Bhattacharyya N. Association of two polymorphisms of DNA polymerase beta in exon-9 and exon-11 with ovarian carcinoma in India. Asian Pac J Cancer Prev. 2012;13(4):1321–4.PubMedCrossRef Khanra K, Panda K, Bhattacharya C, Mitra AK, Sarkar R, Bhattacharyya N. Association of two polymorphisms of DNA polymerase beta in exon-9 and exon-11 with ovarian carcinoma in India. Asian Pac J Cancer Prev. 2012;13(4):1321–4.PubMedCrossRef
16.
Zurück zum Zitat Khanra K, Bhattacharya C, Bhattacharyya N. Association of a newly identified variant of DNA polymerase beta (polβΔ63–123, 208–304) with the risk factor of ovarian carcinoma in India. Asian Pac J Cancer Prev. 2012;13(5):1999–2002.PubMedCrossRef Khanra K, Bhattacharya C, Bhattacharyya N. Association of a newly identified variant of DNA polymerase beta (polβΔ63–123, 208–304) with the risk factor of ovarian carcinoma in India. Asian Pac J Cancer Prev. 2012;13(5):1999–2002.PubMedCrossRef
17.
Zurück zum Zitat Iwanaga A, Ouchida M, Miyazaki K, Hori K, Mukai T. Functional mutation of DNA polymerase beta found in human gastric cancer–inability of the base excision repair in vitro. Mutat Res. 1999;435(2):121–8.PubMedCrossRef Iwanaga A, Ouchida M, Miyazaki K, Hori K, Mukai T. Functional mutation of DNA polymerase beta found in human gastric cancer–inability of the base excision repair in vitro. Mutat Res. 1999;435(2):121–8.PubMedCrossRef
18.
Zurück zum Zitat Zhao GQ, Wang T, Zhao Q, Yang HY, Tan XH, Dong ZM. Mutation of DNA polymerase beta in esophageal carcinoma of different regions. World J Gastroenterol. 2005;11(30):4618–22.PubMed Zhao GQ, Wang T, Zhao Q, Yang HY, Tan XH, Dong ZM. Mutation of DNA polymerase beta in esophageal carcinoma of different regions. World J Gastroenterol. 2005;11(30):4618–22.PubMed
19.
Zurück zum Zitat Dong Z, Zhao G, Zhao Q, Yang H, Xue L, Tan X, et al. A study of DNA polymerase beta mutation in human esophageal cancer. Zhonghua Yi Xue Za Zhi. 2002;82(13):899–902.PubMed Dong Z, Zhao G, Zhao Q, Yang H, Xue L, Tan X, et al. A study of DNA polymerase beta mutation in human esophageal cancer. Zhonghua Yi Xue Za Zhi. 2002;82(13):899–902.PubMed
20.
Zurück zum Zitat Dong ZM, Zheng NG, Wu JL, Li SK, Wang YL. Difference in expression level and localization of DNA polymerase beta among human esophageal cancer focus, adjacent and corresponding normal tissues. Dis Esophagus. 2006;19(3):172–6.PubMedCrossRef Dong ZM, Zheng NG, Wu JL, Li SK, Wang YL. Difference in expression level and localization of DNA polymerase beta among human esophageal cancer focus, adjacent and corresponding normal tissues. Dis Esophagus. 2006;19(3):172–6.PubMedCrossRef
21.
Zurück zum Zitat Li M, Zang W, Wang Y, Li Y, Ma Y, Wang N, et al. DNA polymerase β promoter mutations and transcriptional activity in esophageal squamous cell carcinoma. Tumour Biol. 2013. doi:10.1007/s13277-013-0898-5. Li M, Zang W, Wang Y, Li Y, Ma Y, Wang N, et al. DNA polymerase β promoter mutations and transcriptional activity in esophageal squamous cell carcinoma. Tumour Biol. 2013. doi:10.​1007/​s13277-013-0898-5.
22.
Zurück zum Zitat Wang T, Zang W, Ma Y, Li M, Xuan X, Wang N, et al. DNA polymerase beta promoter mutations affect gene transcription, translation and the sensitivity of esophageal cancer cells to cisplatin treatment. Mol Biol Rep. 2013;40(2):1333–9.PubMedCrossRef Wang T, Zang W, Ma Y, Li M, Xuan X, Wang N, et al. DNA polymerase beta promoter mutations affect gene transcription, translation and the sensitivity of esophageal cancer cells to cisplatin treatment. Mol Biol Rep. 2013;40(2):1333–9.PubMedCrossRef
23.
Zurück zum Zitat Holmes RS, Vaughan TL. Epidemiology and pathogenesis of esophageal cancer. Semin Radiat Oncol. 2007;17(1):2–9.PubMedCrossRef Holmes RS, Vaughan TL. Epidemiology and pathogenesis of esophageal cancer. Semin Radiat Oncol. 2007;17(1):2–9.PubMedCrossRef
24.
Zurück zum Zitat Qi YJ, Chao WX, Chiu JF. An overview of esophageal squamous cell carcinoma proteomics. J Proteomics. 2012;75(11):3129–37.PubMedCrossRef Qi YJ, Chao WX, Chiu JF. An overview of esophageal squamous cell carcinoma proteomics. J Proteomics. 2012;75(11):3129–37.PubMedCrossRef
25.
Zurück zum Zitat Ke L. Mortality and incidence trends from esophagus cancer in selected geographic areas of China circa 1970–90. Int J Cancer. 2002;102(3):271–4.PubMedCrossRef Ke L. Mortality and incidence trends from esophagus cancer in selected geographic areas of China circa 1970–90. Int J Cancer. 2002;102(3):271–4.PubMedCrossRef
26.
Zurück zum Zitat Deziel NC, Wei WQ, Abnet CC, Qiao YL, Sunderland D, Ren JS, et al. A multi-day environmental study of polycyclic aromatic hydrocarbon exposure in a high-risk region for esophageal cancer in China. J Expo Sci Environ Epidemiol. 2013;23(1):52–9.PubMedCentralPubMedCrossRef Deziel NC, Wei WQ, Abnet CC, Qiao YL, Sunderland D, Ren JS, et al. A multi-day environmental study of polycyclic aromatic hydrocarbon exposure in a high-risk region for esophageal cancer in China. J Expo Sci Environ Epidemiol. 2013;23(1):52–9.PubMedCentralPubMedCrossRef
27.
28.
Zurück zum Zitat Li LW, Li YY, Li XY, Zhang CP, Zhou Y, Lu SH. A novel tumor suppressor gene ECRG4 interacts directly with TMPRSS11A (ECRG1) to inhibit cancer cell growth in esophageal carcinoma. BMC Cancer. 2011;11:52.PubMedCentralPubMedCrossRef Li LW, Li YY, Li XY, Zhang CP, Zhou Y, Lu SH. A novel tumor suppressor gene ECRG4 interacts directly with TMPRSS11A (ECRG1) to inhibit cancer cell growth in esophageal carcinoma. BMC Cancer. 2011;11:52.PubMedCentralPubMedCrossRef
29.
Zurück zum Zitat Bhattacharyya N, Banerjee S. A variant of DNA polymerase beta acts as a dominant negative mutant. Proc Natl Acad Sci U S A. 1997;94(19):10324–9.PubMedCentralPubMedCrossRef Bhattacharyya N, Banerjee S. A variant of DNA polymerase beta acts as a dominant negative mutant. Proc Natl Acad Sci U S A. 1997;94(19):10324–9.PubMedCentralPubMedCrossRef
30.
Zurück zum Zitat Guo Z, Zheng L, Dai H, Zhou M, Xu H, Shen B. Human DNA polymerase beta polymorphism, Arg137Gln, impairs its polymerase activity and interaction with PCNA and the cellular base excision repair capacity. Nucleic Acids Res. 2009;37(10):3431–41.PubMedCentralPubMedCrossRef Guo Z, Zheng L, Dai H, Zhou M, Xu H, Shen B. Human DNA polymerase beta polymorphism, Arg137Gln, impairs its polymerase activity and interaction with PCNA and the cellular base excision repair capacity. Nucleic Acids Res. 2009;37(10):3431–41.PubMedCentralPubMedCrossRef
31.
Zurück zum Zitat Yamtich J, Nemec AA, Keh A, Sweasy JB. A germline polymorphism of DNA polymerase beta induces genomic instability and cellular transformation. PLoS Genet. 2012;8(11):e1003052.PubMedCentralPubMedCrossRef Yamtich J, Nemec AA, Keh A, Sweasy JB. A germline polymorphism of DNA polymerase beta induces genomic instability and cellular transformation. PLoS Genet. 2012;8(11):e1003052.PubMedCentralPubMedCrossRef
Metadaten
Titel
DNA polymerase β mutations and survival of patients with esophageal squamous cell carcinoma in Linzhou City, China
verfasst von
Min Li
Wenqiao Zang
Yuanyuan Wang
Yunyun Ma
Xiaoyan Xuan
Jimin Zhao
Lulu Liu
Ziming Dong
Guoqiang Zhao
Publikationsdatum
01.01.2014
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 1/2014
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-013-1077-4

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