Literature DB >> 21861227

XPC mRNA level may predict relapse in never-smokers with non-small cell lung cancers.

Kun-Tu Yeh1, Yi-Hui Wu, Ming-Ching Lee, Lee Wang, Chien-Te Li, Chih-Yi Chen, Huei Lee.   

Abstract

BACKGROUND: Disease recurrence and distant metastasis are the major causes of death in resected non-small cell lung cancer (NSCLC). The prognostic marker for never-smokers with this disease remains to be identified. To improve patient outcome, establishing an adjacent molecular marker to predict relapse of NSCLC in never-smokers is needed.
METHODS: Three hundred two lung tumors from NSCLC patients and normal lung tissues from 68 noncancer subjects were enrolled to evaluate XPC (xeroderma pigmentosum group C) mRNA expression by quantitative real-time reverse transcriptase polymerase chain reaction. Receiver operating characteristic curve analysis was used to search for a feasible cutoff point of XPC mRNA levels for predicting recurrence-free survival. Of the 326 patients, 214 were confirmed as only receiving surgical resection. Kaplan-Meier and multivariate Cox regression analysis were used to assess the prognostic value of XPC mRNA level in lung tumors from patients who only received surgical resection.
RESULTS: Receiver operating characteristic curve analysis indicated 30.28 as a cutoff point, and thus 150 and 64 tumors with low- and high-XPC mRNA expression were categorized in this study population. Low-XPC mRNA appeared with more frequency in never-smokers and in late-stage (stage II-III) disease than smokers and early-stage disease (stage I). Kaplan-Meier analysis indicated that patients with low-XPC mRNA had shorter recurrence-free survival than that found in never-smokers (P = 0.002), but not in smokers (P = 0.296). Cox regression analysis further revealed that low-XPC mRNA may independently predict relapse in lung cancer of never-smokers (hazard ratio 2.34, 95% confidence interval 1.21-4.51, P = 0.011).
CONCLUSIONS: Low-XPC mRNA may predict relapse in lung cancer patients who are never-smokers.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21861227     DOI: 10.1245/s10434-011-1992-9

Source DB:  PubMed          Journal:  Ann Surg Oncol        ISSN: 1068-9265            Impact factor:   5.344


  3 in total

1.  DNA Repair Capacity for Personalizing Risk and Treatment Response - Assay Development and Optimization in Human Peripheral Blood Mononuclear Cells (PBMCs).

Authors:  Nawar Al Nasrallah; Huaxin Zhou; Patricia A Smith; Catherine R Sears
Journal:  DNA Repair (Amst)       Date:  2022-01-19

Review 2.  Xeroderma Pigmentosum Complementation Group C (XPC): Emerging Roles in Non-Dermatologic Malignancies.

Authors:  Nawar Al Nasrallah; Benjamin M Wiese; Catherine R Sears
Journal:  Front Oncol       Date:  2022-04-21       Impact factor: 5.738

3.  Attenuated NER expressions of XPF and XPC associated with smoking are involved in the recurrence of bladder cancer.

Authors:  Jianhong Qiu; Xiangwei Wang; Xiaodong Meng; Yan Zheng; Gang Li; Jiyao Ma; Gang Ye; Yong Li; Jie Li
Journal:  PLoS One       Date:  2014-12-23       Impact factor: 3.240

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.