Orai1-mediated store-operated Ca2+ entry promotes cervical cancer progression through IL-6 signaling

Cervical cancer is a major cause of cancer-associated mortality among women in developing countries. Orai1-mediated store-operated Ca2+ entry (SOCE) is the primary mechanism underlying most of the non-excitable calcium influx into cells. There is at present limited evidence showing that Orai1 can fu...

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Main Authors: Yiyun Pan, Jing Huang, Kang Liu, Chuanhua Xie, Hailong Chen, Zhong Guo, Shoujun Guo, Yijian Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-10-01
Series:Frontiers in Molecular Biosciences
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmolb.2022.1041674/full
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author Yiyun Pan
Yiyun Pan
Jing Huang
Kang Liu
Chuanhua Xie
Hailong Chen
Zhong Guo
Shoujun Guo
Yijian Chen
Yijian Chen
author_facet Yiyun Pan
Yiyun Pan
Jing Huang
Kang Liu
Chuanhua Xie
Hailong Chen
Zhong Guo
Shoujun Guo
Yijian Chen
Yijian Chen
author_sort Yiyun Pan
collection DOAJ
description Cervical cancer is a major cause of cancer-associated mortality among women in developing countries. Orai1-mediated store-operated Ca2+ entry (SOCE) is the primary mechanism underlying most of the non-excitable calcium influx into cells. There is at present limited evidence showing that Orai1 can function as an oncogene or a tumor suppressor depending on the cancer type. Furthermore, the exact biological functions of Orai1 in cervical cancer and the underlying mechanisms are still poorly understood. In this study, we found that Orai1 was upregulated in cervical cancer tissues, and promoted the growth of human cervical cancer cells both in vitro and in vivo. Gene silencing of Orai1 in cervical cancer cells significantly decreased interleukin (IL)-6 secretion. Interestingly, exogenous IL-6 abrogated the effects of Orai1 silencing and restored the clonogenicity of cervical cancer cells. Furthermore, we also observed a positive correlation between Orai1 and IL-6 expression in human cervical cancer samples. Taken together, our findings indicate that Orai1 functions as an oncogene in cervical cancer and is a promising therapeutic target.
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spelling doaj.art-058a10d061ba4740981dfa0a55a615582022-12-22T03:32:21ZengFrontiers Media S.A.Frontiers in Molecular Biosciences2296-889X2022-10-01910.3389/fmolb.2022.10416741041674Orai1-mediated store-operated Ca2+ entry promotes cervical cancer progression through IL-6 signalingYiyun Pan0Yiyun Pan1Jing Huang2Kang Liu3Chuanhua Xie4Hailong Chen5Zhong Guo6Shoujun Guo7Yijian Chen8Yijian Chen9Suzhou Medical College of Soochow University, Suzhou, Jiangsu, ChinaGanzhou Cancer Hospital, Ganzhou, Jiangxi, ChinaGanzhou Cancer Hospital, Ganzhou, Jiangxi, ChinaThe First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, ChinaGanzhou Cancer Hospital, Ganzhou, Jiangxi, ChinaGanzhou Cancer Hospital, Ganzhou, Jiangxi, ChinaThe First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, ChinaGanzhou Cancer Hospital, Ganzhou, Jiangxi, ChinaSuzhou Medical College of Soochow University, Suzhou, Jiangsu, ChinaThe First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, ChinaCervical cancer is a major cause of cancer-associated mortality among women in developing countries. Orai1-mediated store-operated Ca2+ entry (SOCE) is the primary mechanism underlying most of the non-excitable calcium influx into cells. There is at present limited evidence showing that Orai1 can function as an oncogene or a tumor suppressor depending on the cancer type. Furthermore, the exact biological functions of Orai1 in cervical cancer and the underlying mechanisms are still poorly understood. In this study, we found that Orai1 was upregulated in cervical cancer tissues, and promoted the growth of human cervical cancer cells both in vitro and in vivo. Gene silencing of Orai1 in cervical cancer cells significantly decreased interleukin (IL)-6 secretion. Interestingly, exogenous IL-6 abrogated the effects of Orai1 silencing and restored the clonogenicity of cervical cancer cells. Furthermore, we also observed a positive correlation between Orai1 and IL-6 expression in human cervical cancer samples. Taken together, our findings indicate that Orai1 functions as an oncogene in cervical cancer and is a promising therapeutic target.https://www.frontiersin.org/articles/10.3389/fmolb.2022.1041674/fullOrai1SOCEcervical cancerIL-6progression
spellingShingle Yiyun Pan
Yiyun Pan
Jing Huang
Kang Liu
Chuanhua Xie
Hailong Chen
Zhong Guo
Shoujun Guo
Yijian Chen
Yijian Chen
Orai1-mediated store-operated Ca2+ entry promotes cervical cancer progression through IL-6 signaling
Frontiers in Molecular Biosciences
Orai1
SOCE
cervical cancer
IL-6
progression
title Orai1-mediated store-operated Ca2+ entry promotes cervical cancer progression through IL-6 signaling
title_full Orai1-mediated store-operated Ca2+ entry promotes cervical cancer progression through IL-6 signaling
title_fullStr Orai1-mediated store-operated Ca2+ entry promotes cervical cancer progression through IL-6 signaling
title_full_unstemmed Orai1-mediated store-operated Ca2+ entry promotes cervical cancer progression through IL-6 signaling
title_short Orai1-mediated store-operated Ca2+ entry promotes cervical cancer progression through IL-6 signaling
title_sort orai1 mediated store operated ca2 entry promotes cervical cancer progression through il 6 signaling
topic Orai1
SOCE
cervical cancer
IL-6
progression
url https://www.frontiersin.org/articles/10.3389/fmolb.2022.1041674/full
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