Email this article Impact of HNF4α disrupted expression on hepatocellular carcinoma cells sensitivity to oncogenic pathways inhibitors
- Authors: Makarova A.S.1, Krivtsova O.M.2,3, Chesnokov M.S.1, Lazarevich N.I.2,3
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Affiliations:
- Research Institute of Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia.
- Research Institute of Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia
- Biological Faculty, M.V. Lomonosov Moscow State University.
- Issue: Vol 4, No 3 (2017)
- Pages: 83-91
- Section: RESEARCH ARTICLES
- Published: 16.10.2017
- URL: https://umo.abvpress.ru/jour/article/view/105
- DOI: https://doi.org/10.17650/2313-805X-2017-4-3-83-91
- ID: 105
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Abstract
Introduction. Hepatocellular carcinoma (HCC) is characterized by aggressive course, high lethality rate and resistance to current systemic treatment. Analysis of molecular aberrations associated with HCC pathogenesis that control biological properties of HCC allows to evaluate potential efficacy of inhibiting certain oncogenic cascades. The present study is focused on investigation of the impact of reduced expression of the key hepatocyte differentiation regulator, HNF4α, often downregulated in HCC, that influences sensitivity of HCC cells to inhibitors of the major oncogenic pathways mTOR, CDK4/6-pRb and ROCK.
Materials and methods. Changes in cells proliferation and migration caused by HNF4А gene stable knockdown were tested in human HCC cell cultures HepG2 and Huh7 followed by examination of these cellular properties under mTOR (rapamycin), CDK4/6 (PD0332991, palbociclib) and ROCK 1/2 (Y27632) inhibitors treatment. Gene expression levels were estimated by the real-time polymerase chain reaction method (Real-Time PCR).
Results. HNF4А gene knockdown alters HepG2 and Huh7 cell migration associated with E-cadherin and N-cadherin expression changes. The HNF4α repression weakens Y27632-induced blockade of HCC cells migration potential. HNF4А gene knockdown causes resistance of Huh7 cells and increase of HepG2 cells sensitivity to rapamycin and PD0332991 that block cells migration ability.
Conclusions. Expression level of HNF4α renders influence on migration of HCC cells and contributes to their sensitivity to mTOR, CDK4/6 and ROCK1/2 inhibitors’ impact on cell migration activity.
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About the authors
A. S. Makarova
Research Institute of Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia.
Author for correspondence.
Email: fake@neicon.ru
24 Kashirskoe Shosse, Moscow 115478. Russian Federation
O. M. Krivtsova
Research Institute of Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; Biological Faculty, M.V. Lomonosov Moscow State University.
Email: fake@neicon.ru
Build. 12, 1 Leninskie Gory, Moscow 119234. Russian Federation
M. S. Chesnokov
Research Institute of Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia.
Email: fake@neicon.ru
24 Kashirskoe Shosse, Moscow 115478. Russian Federation
N. I. Lazarevich
Research Institute of Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; Biological Faculty, M.V. Lomonosov Moscow State University.
Email: lazarevich.nl@gmail.com
Build. 12, 1 Leninskie Gory, Moscow 119234. Russian Federation
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