Knockdown of CARD14 Inhibits Cell Proliferation and Migration in Breast Cancer Cells.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 17 02 2020
revised: 24 02 2020
accepted: 25 02 2020
entrez: 3 4 2020
pubmed: 3 4 2020
medline: 10 4 2020
Statut: ppublish

Résumé

Caspase recruitment domain family, member 14 (CARD14) is a member of the CARD family of proteins, which play an important role in immune and inflammatory response, and cell survival and proliferation. Here, we identified the role of CARD14 in human breast cancer. Immunohistochemistry was performed to evaluate CARD14 expression in breast cancer. Using CARD14 knockdown cells by small interfering RNA, colony formation and MTT assays, flow cytometry analyses, and migration assays were performed to evaluate the proliferation, cell cycle distribution, apoptosis, and migration ability of MCF7 and SK-BR-3 cells. CARD14 expression was significantly higher in breast cancer samples than in normal breast samples. CARD14 knockdown inhibited cell proliferation and migration, caused cell cycle arrest at the G CARD14 regulates the proliferation and migration of MCF7 and SK-BR-3 cells; it is thus, a novel potential therapeutic target in breast cancer.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Caspase recruitment domain family, member 14 (CARD14) is a member of the CARD family of proteins, which play an important role in immune and inflammatory response, and cell survival and proliferation. Here, we identified the role of CARD14 in human breast cancer.
MATERIALS AND METHODS METHODS
Immunohistochemistry was performed to evaluate CARD14 expression in breast cancer. Using CARD14 knockdown cells by small interfering RNA, colony formation and MTT assays, flow cytometry analyses, and migration assays were performed to evaluate the proliferation, cell cycle distribution, apoptosis, and migration ability of MCF7 and SK-BR-3 cells.
RESULTS RESULTS
CARD14 expression was significantly higher in breast cancer samples than in normal breast samples. CARD14 knockdown inhibited cell proliferation and migration, caused cell cycle arrest at the G
CONCLUSION CONCLUSIONS
CARD14 regulates the proliferation and migration of MCF7 and SK-BR-3 cells; it is thus, a novel potential therapeutic target in breast cancer.

Identifiants

pubmed: 32234884
pii: 40/4/1953
doi: 10.21873/anticanres.14150
doi:

Substances chimiques

CARD Signaling Adaptor Proteins 0
Membrane Proteins 0
RNA, Small Interfering 0
CARD14 protein, human EC 4.6.1.-
Guanylate Cyclase EC 4.6.1.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1953-1962

Informations de copyright

Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Ji-Yeon Lim (JY)

Department of Premedical Sciences, College of Medicine, Chosun University, Gwangju, Republic of Korea.

Seok Won Kim (SW)

Department of Neurosurgery, College of Medicine, Chosun University, Gwangju, Republic of Korea.

Byeol Kim (B)

Department of Premedical Sciences, College of Medicine, Chosun University, Gwangju, Republic of Korea.

Seon-Joo Park (SJ)

Department of Premedical Sciences, College of Medicine, Chosun University, Gwangju, Republic of Korea parksj@chosun.ac.kr.

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Classifications MeSH