Evidence map›Paper›PMID 40676600›Full record

ArticleBMC cancer2025

Alterations and correlation between DNA damage and repair response and PD-L1 expression in non-small cell lung cancers.

Jiali Peng, Jiayu Zhou, Gang Liu, Poming Kang, Xi Tang, Ziyue Luo, Yu Jiang

Abstract read
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Jiali Peng *Department of Respiratory and Critical Care Medicine, The University-Town Hospital of Chongqing Medical University, Chongqing, 401331, P.R. China.
Jiayu Zhou *Department of Respiratory and Critical Care Medicine, The University-Town Hospital of Chongqing Medical University, Chongqing, 401331, P.R. China.
Gang LiuDepartment of Critical Care Medicine, The University-Town Hospital of Chongqing Medical University, Chongqing, 401331, P.R. China.
Poming KangDepartment of thoracic surgery, The University-Town Hospital of Chongqing Medical University, Chongqing, 401331, P.R. China.
Xi TangDepartment of Respiratory and Critical Care Medicine, The University-Town Hospital of Chongqing Medical University, Chongqing, 401331, P.R. China.
Ziyue LuoDepartment of Respiratory and Critical Care Medicine, The University-Town Hospital of Chongqing Medical University, Chongqing, 401331, P.R. China.
Yu JiangDepartment of Respiratory and Critical Care Medicine, The University-Town Hospital of Chongqing Medical University, Chongqing, 401331, P.R. China. jiangyu@cqmu.edu.cn.

Funding

Project of Chongqing Natural Science Foundation Committee cstc2020jcyj-msxmX0359
6 · The paper itself

Abstract

backgroundDNA damage and repair (DDR) is involved in the antitumor immune response, however, the correlation between DNA damage response with immunotherapy in NSCLC remain unclear. We examined the relationship between DDR alterations and expression of PD-L1 in non-small cell lung cancer.

methodsTumor tissues, para-carcinoma and normal tissues, were obtained from 54 patients who were surgically resected NSCLC tumors. Patient characteristics, neoplasm staging and pathological information were collected. Immunohistochemical analysis of tissue samples was analyzed for γH2AX、RAD51, PARP-1 and PD-L1 protein expression.

resultsA total of 54 patients with non-small cell lung cancer were included in this study, including 24 males and 30 females with ages ranging from 45 to 79 years (mean, 63.5 years). The high expression rate of γH2AX staining in lung cancer was 81.5%(44/54)and the expression levels of γH2AX protein were significantly higher in NSCLC than those in paired para-carcinoma 50%(27/54) and normal tissues 42.6%(23/54). The expression levels of RAD51 protein were significantly higher in lung cancer tissue 68.5%(37/54) than those in paired para-carcinoma 48.1%(26/54) and normal tissues 40.7%(22/54). There was a significant correlation between high RAD51 expression and male patients 87.5%(21/24) (p = 0.009) and a history of smoking 90%(18/20) (p = 0.014). The presence of any DDR alteration was showed with PD-L1. (1) HigherγH2AX expression was observed in the PD-L1 positive cases 90.6% (29/32) compared to the PD-L1 negative cases 68.2% (15/22). Lung cancers with higher γH2AX expression were associated with the higher expression of PD-L1 (p = 0.046, r = 0.284). (2) There was no statistically significant correlation between expression of PD-L1 and RAD51 (p = 0.221, r = 0.168). (3) Higher PARP-1 expression was observed in the PD-L1 negative cases 59.1% (13/22) compared to the PD-L1 positive cases 25% (8/32). Lung cancers with higher PARP-1 expression were associated with the lower expression of PD-L1 (p = 0.009, r=-0.344). (4) No statistically significant association was observed in relationship between expression of DDR Expression (γH2AX、RAD51) and PARP-1 of patients (p = 0.507 and p = 0.817,respectively).

conclusionOverall, our study shows that high expression of γH2AX, RAD51, and PARP1 proteins display in NSCLC and proves that DNA damage repair may be closely related to the occurrence and development of NSCLC. γH2AX could be a predictor of the adaptation of ICIs as an alternative to PD-L1, and NSCLC is expected to benefit from PARP-1 inhibitors combined with immunotherapy.

Indexed as

B7-H1 AntigenCarcinoma, Non-Small-Cell LungDNA DamageDNA RepairLung NeoplasmsAgedBiomarkers, TumorFemaleHistonesHumansImmunohistochemistryMaleMiddle AgedNeoplasm StagingPoly (ADP-Ribose) Polymerase-1Rad51 RecombinaseB7-H1 AntigenBiomarkers, TumorCD274 protein, humanH2AX protein, humanHistonesPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1RAD51 protein, humanRad51 RecombinaseDNA damage and repairNon-small cell lung cancer (NSCLC)PD-L1

Identifiers

PMID40676600
PMCPMC12273298

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