NRIP1 regulates cell proliferation in lung adenocarcinoma cells

Author:

Watanabe Fumihiko12,Sato Shigemitsu13,Hirose Takuo134ORCID,Endo Moe1,Endo Akari14,Ito Hiroki14,Ohba Koji1,Mori Takefumi34,Takahashi Kazuhiro1ORCID

Affiliation:

1. Tohoku University Graduate School of Medicine Department of Endocrinology and Applied Medical Science, , 2-1, Seiryo, Aoba, 980-8575 Sendai, Japan

2. Fukushima Medical University School of Medicine Department of Blood Transfusion and Transplantation Immunology, , 1, Hikarigaoka, Fukushima, 960-1295 Fukushima, Japan

3. Tohoku Medical and Pharmaceutical University Division of Integrative Renal Replacement Therapy, Faculty of Medicine, , 1-15-1, Fukumuro, Miyagino, 983-8536 Sendai, Japan

4. Tohoku Medical and Pharmaceutical University Division of Nephrology and Endocrinology, Faculty of Medicine, , 1-15-1, Fukumuro, Miyagino, 983-8536 Sendai, Japan

Abstract

Abstract Nuclear receptor interacting protein 1 (NRIP1) is a transcription cofactor that regulates the activity of nuclear receptors and transcription factors. Functional expression of NRIP1 has been identified in multiple cancers. However, the expression and function of NRIP1 in lung adenocarcinoma have remained unclear. Thus, we aimed to clarify the NRIP1 expression and its functions in lung adenocarcinoma cells. NRIP1 and Ki-67 were immunostained in the tissue microarray section consisting of 64 lung adenocarcinoma cases, and the association of NRIP1 immunoreactivity with clinical phenotypes was examined. Survival analysis was performed in lung adenocarcinoma data from The Cancer Genome Atlas (TCGA). Human A549 lung adenocarcinoma cell line with an NRIP1-silencing technique was used in vitro study. Forty-three of 64 cases were immunostained with NRIP1. Ki-67–positive cases were more frequent in NRIP1-positive cases as opposed to NRIP1-negative cases. Higher NRIP1 mRNA expression was associated with poor prognosis in the TCGA lung adenocarcinoma data. NRIP1 was mainly located in the nucleus of A549 cells. NRIP1 silencing significantly reduced the number of living cells, suppressed cell proliferation, and induced apoptosis. These results suggest that NRIP1 participates in the progression and development of lung adenocarcinoma. Targeting NRIP1 may be a possible therapeutic strategy against lung adenocarcinoma.

Funder

The Mochida Memorial Foundation for Medical and Pharmaceutical Research

Takeda Research Foundation

Ministry of Education, Culture, Sports, Science and Technology of Japan

Grants-in-Aid for Scientific Research

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Biochemistry,General Medicine

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