4.3 Article

Correlation between serum IL-1β and miR-144-3p as well as their prognostic values in LUAD and LUSC patients

期刊

ONCOTARGET
卷 7, 期 52, 页码 85876-85887

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.13042

关键词

LUAD; LUSC; IL-1 beta; miR-144-3p; prognosis

资金

  1. National Key Technology RD Program [2015BAI12B12]
  2. National Natural Science Foundation of China [81171653, 81302047, 31428005]
  3. Natural science fundation of Jiangsu Province [BE2016660, BK20130243]
  4. Changzhou Science and Technology Project (Applied Based Research) [CJ20159021]
  5. Research support plan for post-doctor of Jiangsu Province [1601088C]

向作者/读者索取更多资源

Background: IL-1 beta is an essential factor of inflammation initiation, and it also promotes malignant transformation, indicating its tumorigenic property. We aimed to investigate the correlation between IL-1 beta and miR-144-3p as well as their prognostic values in LUAD and LUSC patients. Results: The IL-1 beta level in both LUAD and LUSC patients was significantly higher than that of healthy donors (P < 0.001). In both populations, patients with low IL-1 beta level had better prognosis than high IL-1 beta level (P < 0.001 and P = 0.010, respectively). In A549 cells, miR-144 showed the biggest expression change (-4.38 fold) after IL-1 beta exposure. In LUAD patients, a negative correlation was detected between IL-1 beta and miR-144-3p (r = -0.540, P < 0.001) and the high miR-144-3p group had better prognosis (P = 0.003), which was validated by TCGA data. Clinical stage, IL-1 beta and miR-144-3p were independent risk factors in LUAD patients. In vitro, IL-1 beta and miR-144-3p antagomir could enhance proliferation and miR-144-3p mimics would attenuate the promoting effect of IL-1 beta. Materials and Methods: ELISA and qRT-PCR were applied respectively to detected cytokines and miR-144-3p in 129 LUAD, 54 LUSC and 40 healthy donors. Moreover, miRNA array was carried out for miRNA profiling. TCGA database was employed for validation, and follow up data were collected for prognosis evaluation. MTT assay and western-blot were carried out for proliferation evaluation. Conclusions: In LUAD patients, the serum IL-1 beta level was correlated with miR-144- 3p may affect miR-144-3p at transcriptional level. Both of them were independent risk factors for LUAD prognosis. In addition, IL-1 beta and miR-144-3p might mediate inflammation-promoted tumorigenesis in LUAD patients.

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