SULF2 promotes tumorigenesis and inhibits apoptosis of cervical cancer cells through the ERK/AKT signaling pathway

The objective of this study was to explore the role of the SULF2-mediated ERK/AKT signaling pathway in cervical cancer. SULF2 expression was detected in tumor tissues and tumor-adjacent normal tissues from cervical cancer patients. HeLa cells were divided into six groups: control group, NC group, SU...

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Main Authors: Tao Jiang, Zhao-Hui Chen, Zhe Chen, Dan Tan
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2020-02-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2020000200608&tlng=en
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author Tao Jiang
Zhao-Hui Chen
Zhe Chen
Dan Tan
author_facet Tao Jiang
Zhao-Hui Chen
Zhe Chen
Dan Tan
author_sort Tao Jiang
collection DOAJ
description The objective of this study was to explore the role of the SULF2-mediated ERK/AKT signaling pathway in cervical cancer. SULF2 expression was detected in tumor tissues and tumor-adjacent normal tissues from cervical cancer patients. HeLa cells were divided into six groups: control group, NC group, SULF2 siRNA group, SULF2 group, SULF2 + LY294002 group, and SULF2 + U0125 group. In each group, HeLa cells received the corresponding treatment, followed by measurement of the cellular biological characteristics and expression of the ERK/AKT signaling pathway. We also confirmed the effect of SULF2 in vivo using a xenograft model in nude mice. SULF2 was upregulated in cervical cancer tissues, which was specifically associated with the clinical stage, histological differentiation, and lymphatic metastasis. Compared to the control group, the SULF2 siRNA group displayed decreased expression of SULF2, concomitant with reduced proliferation, migration, and invasion, but there was an increase in the apoptosis rate of HeLa cells, as well as downregulation of the p-Akt/Akt, p-ERK/ERK, and Bax/Bcl-2 ratios and cyclin D1. Additionally, tumor growth was significantly inhibited in the xenograft model of nude mice. The results in the SULF2 group were quite the opposite in which SULF2 facilitated the growth of cervical cancer cells, which was reversed by LY294002 or U0126. SULF2 is highly expressed in cervical cancer, and thus, downregulation of SULF2 can inhibit the ERK1/2 and AKT signaling pathways to suppress the proliferation, invasion, and migration of cervical cancer cells while facilitating apoptosis.
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spelling doaj.art-c59ed4002e654d16af200b0877aaf9652022-12-22T04:13:44ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research1414-431X2020-02-0153210.1590/1414-431x20198901SULF2 promotes tumorigenesis and inhibits apoptosis of cervical cancer cells through the ERK/AKT signaling pathwayTao Jianghttps://orcid.org/0000-0001-8132-8945Zhao-Hui Chenhttps://orcid.org/0000-0002-1723-6138Zhe Chenhttps://orcid.org/0000-0001-8036-8072Dan Tanhttps://orcid.org/0000-0003-4782-7972The objective of this study was to explore the role of the SULF2-mediated ERK/AKT signaling pathway in cervical cancer. SULF2 expression was detected in tumor tissues and tumor-adjacent normal tissues from cervical cancer patients. HeLa cells were divided into six groups: control group, NC group, SULF2 siRNA group, SULF2 group, SULF2 + LY294002 group, and SULF2 + U0125 group. In each group, HeLa cells received the corresponding treatment, followed by measurement of the cellular biological characteristics and expression of the ERK/AKT signaling pathway. We also confirmed the effect of SULF2 in vivo using a xenograft model in nude mice. SULF2 was upregulated in cervical cancer tissues, which was specifically associated with the clinical stage, histological differentiation, and lymphatic metastasis. Compared to the control group, the SULF2 siRNA group displayed decreased expression of SULF2, concomitant with reduced proliferation, migration, and invasion, but there was an increase in the apoptosis rate of HeLa cells, as well as downregulation of the p-Akt/Akt, p-ERK/ERK, and Bax/Bcl-2 ratios and cyclin D1. Additionally, tumor growth was significantly inhibited in the xenograft model of nude mice. The results in the SULF2 group were quite the opposite in which SULF2 facilitated the growth of cervical cancer cells, which was reversed by LY294002 or U0126. SULF2 is highly expressed in cervical cancer, and thus, downregulation of SULF2 can inhibit the ERK1/2 and AKT signaling pathways to suppress the proliferation, invasion, and migration of cervical cancer cells while facilitating apoptosis.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2020000200608&tlng=enSULF2Cervical cancerERK/AKTProliferationApoptosis
spellingShingle Tao Jiang
Zhao-Hui Chen
Zhe Chen
Dan Tan
SULF2 promotes tumorigenesis and inhibits apoptosis of cervical cancer cells through the ERK/AKT signaling pathway
Brazilian Journal of Medical and Biological Research
SULF2
Cervical cancer
ERK/AKT
Proliferation
Apoptosis
title SULF2 promotes tumorigenesis and inhibits apoptosis of cervical cancer cells through the ERK/AKT signaling pathway
title_full SULF2 promotes tumorigenesis and inhibits apoptosis of cervical cancer cells through the ERK/AKT signaling pathway
title_fullStr SULF2 promotes tumorigenesis and inhibits apoptosis of cervical cancer cells through the ERK/AKT signaling pathway
title_full_unstemmed SULF2 promotes tumorigenesis and inhibits apoptosis of cervical cancer cells through the ERK/AKT signaling pathway
title_short SULF2 promotes tumorigenesis and inhibits apoptosis of cervical cancer cells through the ERK/AKT signaling pathway
title_sort sulf2 promotes tumorigenesis and inhibits apoptosis of cervical cancer cells through the erk akt signaling pathway
topic SULF2
Cervical cancer
ERK/AKT
Proliferation
Apoptosis
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2020000200608&tlng=en
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AT zhaohuichen sulf2promotestumorigenesisandinhibitsapoptosisofcervicalcancercellsthroughtheerkaktsignalingpathway
AT zhechen sulf2promotestumorigenesisandinhibitsapoptosisofcervicalcancercellsthroughtheerkaktsignalingpathway
AT dantan sulf2promotestumorigenesisandinhibitsapoptosisofcervicalcancercellsthroughtheerkaktsignalingpathway