REV3L, a promising target in regulating the chemosensitivity of cervical cancer cells.

REV3L, the catalytic subunit of DNA Polymerase ζ (Polζ), plays a significant role in the DNA damage tolerance mechanism of translesion synthesis (TLS). The role of REV3L in chemosensitivity of cervical cancer needs exploration. In the present study, we evaluated the expression of the Polζ protein in...

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Main Authors: Li Yang, Tingyan Shi, Fei Liu, Chunxia Ren, Ziliang Wang, Yingyi Li, Xiaoyu Tu, Gong Yang, Xi Cheng
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4364373?pdf=render
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spelling doaj-7f0f5b8bd3724be68c5c6e644ddfe1af2020-11-25T00:50:46ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e012033410.1371/journal.pone.0120334REV3L, a promising target in regulating the chemosensitivity of cervical cancer cells.Li YangTingyan ShiFei LiuChunxia RenZiliang WangYingyi LiXiaoyu TuGong YangXi ChengREV3L, the catalytic subunit of DNA Polymerase ζ (Polζ), plays a significant role in the DNA damage tolerance mechanism of translesion synthesis (TLS). The role of REV3L in chemosensitivity of cervical cancer needs exploration. In the present study, we evaluated the expression of the Polζ protein in paraffin-embedded tissues using immunohistochemistry and found that the expression of Polζ in cervical cancer tissues was higher than that in normal tissues. We then established some cervical cancer cell lines with REV3L suppression or overexpression. Depletion of REV3L suppresses cell proliferation and colony formation of cervical cancer cells through G1 arrest, and REV3L promotes cell proliferation and colony formation of cervical cancer cells by promoting G1 phase to S phase transition. The suppression of REV3L expression enhanced the sensitivity of cervical cancer cells to cisplatin, and the overexpression of REV3L conferred resistance to cisplatin as evidenced by the alteration of apoptosis rates, and significantly expression level changes of anti-apoptotic proteins B-cell lymphoma 2 (Bcl-2), myeloid cell leukemia sequence 1 (Mcl-1) and B-cell lymphoma-extra large (Bcl-xl) and proapoptotic Bcl-2-associated x protein (Bax). Our data suggest that REV3L plays an important role in regulating cervical cancer cellular response to cisplatin, and thus targeting REV3L may be a promising way to alter chemosensitivity in cervical cancer patients.http://europepmc.org/articles/PMC4364373?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Li Yang
Tingyan Shi
Fei Liu
Chunxia Ren
Ziliang Wang
Yingyi Li
Xiaoyu Tu
Gong Yang
Xi Cheng
spellingShingle Li Yang
Tingyan Shi
Fei Liu
Chunxia Ren
Ziliang Wang
Yingyi Li
Xiaoyu Tu
Gong Yang
Xi Cheng
REV3L, a promising target in regulating the chemosensitivity of cervical cancer cells.
PLoS ONE
author_facet Li Yang
Tingyan Shi
Fei Liu
Chunxia Ren
Ziliang Wang
Yingyi Li
Xiaoyu Tu
Gong Yang
Xi Cheng
author_sort Li Yang
title REV3L, a promising target in regulating the chemosensitivity of cervical cancer cells.
title_short REV3L, a promising target in regulating the chemosensitivity of cervical cancer cells.
title_full REV3L, a promising target in regulating the chemosensitivity of cervical cancer cells.
title_fullStr REV3L, a promising target in regulating the chemosensitivity of cervical cancer cells.
title_full_unstemmed REV3L, a promising target in regulating the chemosensitivity of cervical cancer cells.
title_sort rev3l, a promising target in regulating the chemosensitivity of cervical cancer cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description REV3L, the catalytic subunit of DNA Polymerase ζ (Polζ), plays a significant role in the DNA damage tolerance mechanism of translesion synthesis (TLS). The role of REV3L in chemosensitivity of cervical cancer needs exploration. In the present study, we evaluated the expression of the Polζ protein in paraffin-embedded tissues using immunohistochemistry and found that the expression of Polζ in cervical cancer tissues was higher than that in normal tissues. We then established some cervical cancer cell lines with REV3L suppression or overexpression. Depletion of REV3L suppresses cell proliferation and colony formation of cervical cancer cells through G1 arrest, and REV3L promotes cell proliferation and colony formation of cervical cancer cells by promoting G1 phase to S phase transition. The suppression of REV3L expression enhanced the sensitivity of cervical cancer cells to cisplatin, and the overexpression of REV3L conferred resistance to cisplatin as evidenced by the alteration of apoptosis rates, and significantly expression level changes of anti-apoptotic proteins B-cell lymphoma 2 (Bcl-2), myeloid cell leukemia sequence 1 (Mcl-1) and B-cell lymphoma-extra large (Bcl-xl) and proapoptotic Bcl-2-associated x protein (Bax). Our data suggest that REV3L plays an important role in regulating cervical cancer cellular response to cisplatin, and thus targeting REV3L may be a promising way to alter chemosensitivity in cervical cancer patients.
url http://europepmc.org/articles/PMC4364373?pdf=render
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