Predictive Impact of Common Variations in DNA Repair Genes on Clinical Outcome of Osteosarcoma

被引:27
作者
Bai, Sheng-Bin [1 ,4 ]
Chen, Hong-Xiang [2 ]
Bao, Yong-Xing [3 ]
Luo, Xue-Gang [1 ]
Zhong, Jin-Jie [4 ]
机构
[1] Cent S Univ, Xiangya Sch Med, Dept Anat & Neurobiol, Changsha, Hunan, Peoples R China
[2] People Hosp Xinjiang Autonomous Reg, Dept Gynecol, Urumqi, Peoples R China
[3] Xinjiang Med Univ, Affiliated Hosp 1, Dept Tumor Ctr, Urumqi, Peoples R China
[4] Xinjiang Med Univ, Dept Histol & Embryol, Urumqi, Peoples R China
关键词
XPG; MMS19L; osteosarcoma; clinical outcome; NUCLEOTIDE EXCISION-REPAIR; LUNG-CANCER; POLYMORPHISMS; CHEMOTHERAPY; TOXICITY; ERCC5; XPG; TRANSCRIPTION; CYTOTOXICITY; RISK;
D O I
10.7314/APJCP.2013.14.6.3677
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
We aimed to assess the role of XPG, XPC and MMS19L polymorphisms on response to chemotherapy in osteosarcomas, and the clinical outcomes. One hundred and eighty five osteosarcoma patients who were histologically confirmed were enrolled in our study between January 2007 and December 2009. Genotyping of XPG, XPC and MMS19L was performed in a 384-well plate format on the MassARRAY (R) platform. Individuals with XPG TT genotype and T allele were more likely to be better response to chemotherapy than CC genotype, with the OR (95% CI) of 4.17 (1.64-11.54) and 2.66 (1.39-5.11), respectively. Those carrying MMS19L TT genotype and T allele showed better response to chemotherapy, with ORs (95% CI) of 4.8 (1.56-17.7) and 2.3 (1.22-4.36), respectively. Patients carrying TT genotype of XPG and MMS19L showed a significantly longer overall survival than CC genotype, with a 0.47 and 0.30-fold risk of death when compared with the wild-type of the gene. XPG and MMS19L are correlated with response to chemotherapy and prognosis of osteosarcoma, so that they could be used as predictive markers for prognosis.
引用
收藏
页码:3677 / 3680
页数:4
相关论文
共 19 条
[1]
Nucleotide excision repair gene variants and association with survival in osteosarcoma patients treated with neoadjuvant chemotherapy [J].
Biason, P. ;
Hattinger, C. M. ;
Innocenti, F. ;
Talamini, R. ;
Alberghini, M. ;
Scotlandi, K. ;
Zanusso, C. ;
Serra, M. ;
Toffoli, G. .
PHARMACOGENOMICS JOURNAL, 2012, 12 (06) :476-483
[2]
Common variations in ERCC2 are associated with response to cisplatin chemotherapy and clinical outcome in osteosarcoma patients [J].
Caronia, D. ;
Patino-Garcia, A. ;
Milne, R. L. ;
Zalacain-Diez, M. ;
Pita, G. ;
Alonso, M. R. ;
Moreno, L. T. ;
Sierrasesumaga-Ariznabarreta, L. ;
Benitez, J. ;
Gonzalez-Neira, A. .
PHARMACOGENOMICS JOURNAL, 2009, 9 (05) :347-353
[3]
Relationship Between Antimetabolite Toxicity and Pharmacogenetics in Turkish Cancer Patients [J].
Dogan, Mutlu ;
Karabulut, Halil G. ;
Tukun, Ajlan ;
Demirkazik, Ahmet ;
Utkan, Gungor ;
Yalcin, Bulent ;
Dincol, Dilek ;
Akbulut, Hakan ;
Icli, Fikri .
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2012, 13 (04) :1553-1556
[4]
DNA damage and repair [J].
Friedberg, EC .
NATURE, 2003, 421 (6921) :436-440
[5]
Prospective assessment of XPD Lys751Gln and XRCC1 Arg399Gln single nucleotide polymorphisms in lung cancer [J].
Giachino, Daniela F. ;
Ghio, Paolo ;
Regazzoni, Silvia ;
Mandrile, Giorgia ;
Novello, Silvia ;
Selvaggi, Giovanni ;
Gregori, Dario ;
DeMarchi, Mario ;
Scagliotti, Giorgio V. .
CLINICAL CANCER RESEARCH, 2007, 13 (10) :2876-2881
[6]
Role of Endonucleases XPF and XPG in Nucleotide Excision Repair of Platinated DNA and Cisplatin/Oxaliplatin Cytotoxicity [J].
Graf, Nora ;
Ang, Wee Han ;
Zhu, Guangyu ;
Myint, MyatNoeZin ;
Lippard, Stephen J. .
CHEMBIOCHEM, 2011, 12 (07) :1115-1123
[7]
Identification of MMS19 domains with distinct functions in NER and transcription [J].
Hatfield, Melissa D. ;
Reis, Antonio M. C. ;
Obeso, David ;
Cook, James R. ;
Thompson, David M. ;
Rao, Malini ;
Friedberg, Errol C. ;
Queimado, Lurdes .
DNA REPAIR, 2006, 5 (08) :914-924
[8]
Role of ERCC5 promoter polymorphisms in response to platinum-based chemotherapy in patients with advanced non-small-cell lung cancer [J].
He, Caiyun ;
Duan, Zhipeng ;
Li, Ping ;
Xu, Qian ;
Yuan, Yuan .
ANTI-CANCER DRUGS, 2013, 24 (03) :300-305
[9]
ERCC5/XPG, ERCC1, and BRCA1 Gene Status and Clinical Benefit of Trabectedin in Patients With Soft Tissue Sarcoma [J].
Italiano, Antoine ;
Laurand, Armelle ;
Laroche, Audrey ;
Casali, Paolo ;
Sanfilippo, Roberta ;
Le Cesne, Axel ;
Judson, Ian ;
Blay, Jean-Yves ;
Ray-Coquard, Isabelle ;
Bui, Binh ;
Coindre, Jean-Michel ;
Nieto, Antonio ;
Tercero, Juan-Carlos ;
Jimeno, Jose ;
Robert, Jacques ;
Pourquier, Philippe .
CANCER, 2011, 117 (15) :3445-3456
[10]
Irofulven cytotoxicity depends on transcription-coupled nucleotide excision repair and is correlated with XPG expression in solid tumor cells [J].
Koeppel, F ;
Poindessous, V ;
Lazar, V ;
Raymond, E ;
Sarasin, A ;
Larsen, AK .
CLINICAL CANCER RESEARCH, 2004, 10 (16) :5604-5613