4.3 Article

Efficacy of adjuvant chemotherapy for non-small cell lung cancer assessed by metastatic potential associated with ACTN4

期刊

ONCOTARGET
卷 7, 期 22, 页码 33165-33178

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.8890

关键词

ACTN4 (actinin-4); predictive biomarker for adjuvant chemotherapy; early stage of non-small cell lung cancer (NSCLC); JBR. 10

资金

  1. Japan Agency for Medical Research and Development (AMED) of the Ministry of Health, Labour and Welfare of Japan
  2. Ministry of Education, Culture, Sports, Science and Technology (METX) of Japan
  3. National Cancer Center Research and Development Fund [23-A-38, 23-A-11, 23-A-7]
  4. Grants-in-Aid for Scientific Research [15K15751, 23390469] Funding Source: KAKEN

向作者/读者索取更多资源

Although several clinical trials have demonstrated the benefits of platinum-combined adjuvant chemotherapy for resected non-small cell lung cancer (NSCLC), predictive biomarkers for the efficacy of such therapy have not yet been identified. Selection of patients with high metastatic ability in the early stage of non-small cell lung cancer (NSCLC) has the potential to predict clinical benefit of adjuvant chemotherapy (ADJ). In order to develop a predictive biomarker for efficacy of ADJ, we reanalyzed patient data using a public database enrolled by JBR. 10, which was a clinical trial to probe the clinical benefits of ADJ in stage-IB/II patients with NSCLC. The patients who were enrolled by JBR. 10 were classified into 2 subgroups according to expression of the ACTN4 transcript: ACTN4 positive (ACTN4 (+)) and ACTN4 negative (ACTN4 (-)). In the ACTN4 (+) group, overall survival (OS) was significantly higher in the ADJ subgroup compared with the observation subgroup (OBS), indicating a significant survival benefit of ADJ. However, no difference in OS was found between ADJ and OBS groups in ACTN4 (-). Although ACTN4 expression level did not correlate with the chemosensitivity of cancer cell lines for cytotoxic drugs, the metastatic potential of A549 lung adenocarcinoma cells was significantly reduced by ACTN4 shRNA in in vitro assays and in an animal transplantation model. The clinical and preclinical data suggested that ACTN4 is a potential predictive biomarker for efficacy of ADJ in stage-IB/II patients with NSCLC, by reflecting the metastatic potential of tumor cells.

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