INPP4B restrains cell proliferation and metastasis via regulation of the PI3K/AKT/SGK pathway
Cervical cancer continues to be among the most frequent gynaecologic cancers worldwide. The phosphoinositide 3‐kinase (PI3K)/protein kinase B (AKT) pathway is constitutively activated in cervical cancer. Inositol polyphosphate 4‐phosphatase type II (INPP4B) is a phosphoinositide phosphatase and cons...
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Published in | Journal of cellular and molecular medicine Vol. 22; no. 5; pp. 2935 - 2943 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley and Sons Inc
01.05.2018
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Abstract | Cervical cancer continues to be among the most frequent gynaecologic cancers worldwide. The phosphoinositide 3‐kinase (PI3K)/protein kinase B (AKT) pathway is constitutively activated in cervical cancer. Inositol polyphosphate 4‐phosphatase type II (INPP4B) is a phosphoinositide phosphatase and considered a negative regulatory factor of the PI3K/AKT pathway. INPP4B has diverse roles in various tumours, but its role in cervical cancer is largely unknown. In this study, we investigated the role of INPP4B in cervical cancer. Overexpression of INPP4B in HeLa, SiHa and C33a cells inhibited cell proliferation, metastasis and invasiveness in CCK‐8, colony formation, anchorage‐independent growth in soft agar and Transwell assay. INPP4B reduced the expression of some essential proteins in the PI3K/AKT/SGK3 pathway including p‐AKT, p‐SGK3, p‐mTOR, phospho‐p70S6K and PDK1. In addition, overexpression of INPP4B decreased xenograft tumour growth in nude mice. Loss of INPP4B protein expression was found in more than 60% of human cervical carcinoma samples. In conclusion, INPP4B impedes the proliferation and invasiveness of cervical cancer cells by inhibiting the activation of two downstream molecules of the PI3K pathway, AKT and SGK3. INPP4B acts as a tumour suppressor in cervical cancer cells. |
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AbstractList | Cervical cancer continues to be among the most frequent gynaecologic cancers worldwide. The phosphoinositide 3‐kinase (
PI
3K)/protein kinase B (
AKT
) pathway is constitutively activated in cervical cancer. Inositol polyphosphate 4‐phosphatase type
II
(
INPP
4B) is a phosphoinositide phosphatase and considered a negative regulatory factor of the
PI
3K/
AKT
pathway.
INPP
4B has diverse roles in various tumours, but its role in cervical cancer is largely unknown. In this study, we investigated the role of
INPP
4B in cervical cancer. Overexpression of
INPP
4B in HeLa, SiHa and C33a cells inhibited cell proliferation, metastasis and invasiveness in
CCK
‐8, colony formation, anchorage‐independent growth in soft agar and Transwell assay.
INPP
4B reduced the expression of some essential proteins in the
PI
3K/
AKT
/
SGK
3 pathway including p‐
AKT
, p‐
SGK
3, p‐
mTOR
, phospho‐p70S6K and
PDK
1. In addition, overexpression of
INPP
4B decreased xenograft tumour growth in nude mice. Loss of
INPP
4B protein expression was found in more than 60% of human cervical carcinoma samples. In conclusion,
INPP
4B impedes the proliferation and invasiveness of cervical cancer cells by inhibiting the activation of two downstream molecules of the
PI
3K pathway,
AKT
and
SGK
3.
INPP
4B acts as a tumour suppressor in cervical cancer cells. Cervical cancer continues to be among the most frequent gynaecologic cancers worldwide. The phosphoinositide 3‐kinase (PI3K)/protein kinase B (AKT) pathway is constitutively activated in cervical cancer. Inositol polyphosphate 4‐phosphatase type II (INPP4B) is a phosphoinositide phosphatase and considered a negative regulatory factor of the PI3K/AKT pathway. INPP4B has diverse roles in various tumours, but its role in cervical cancer is largely unknown. In this study, we investigated the role of INPP4B in cervical cancer. Overexpression of INPP4B in HeLa, SiHa and C33a cells inhibited cell proliferation, metastasis and invasiveness in CCK‐8, colony formation, anchorage‐independent growth in soft agar and Transwell assay. INPP4B reduced the expression of some essential proteins in the PI3K/AKT/SGK3 pathway including p‐AKT, p‐SGK3, p‐mTOR, phospho‐p70S6K and PDK1. In addition, overexpression of INPP4B decreased xenograft tumour growth in nude mice. Loss of INPP4B protein expression was found in more than 60% of human cervical carcinoma samples. In conclusion, INPP4B impedes the proliferation and invasiveness of cervical cancer cells by inhibiting the activation of two downstream molecules of the PI3K pathway, AKT and SGK3. INPP4B acts as a tumour suppressor in cervical cancer cells. |
Author | Zhang, Weifang Chen, Chunyan Qi, Mei Liu, Juan Zhao, Weiming Chen, Ying Sun, Zeyu Wang, Xiao |
AuthorAffiliation | 3 Department of Hematology Qilu Hospital Shandong University Jinan China 1 Department of Pathogenic Biology Key Laboratory of Infection and Immunity of Shandong Province School of Basic Medical Sciences Shandong University Jinan Shandong China 2 Department of Pathology School of Basic Medical Sciences Shandong University Jinan Shandong China |
AuthorAffiliation_xml | – name: 2 Department of Pathology School of Basic Medical Sciences Shandong University Jinan Shandong China – name: 3 Department of Hematology Qilu Hospital Shandong University Jinan China – name: 1 Department of Pathogenic Biology Key Laboratory of Infection and Immunity of Shandong Province School of Basic Medical Sciences Shandong University Jinan Shandong China |
Author_xml | – sequence: 1 givenname: Ying orcidid: 0000-0001-8218-6889 surname: Chen fullname: Chen, Ying organization: Shandong University – sequence: 2 givenname: Zeyu surname: Sun fullname: Sun, Zeyu organization: Shandong University – sequence: 3 givenname: Mei surname: Qi fullname: Qi, Mei organization: Shandong University – sequence: 4 givenname: Xiao surname: Wang fullname: Wang, Xiao organization: Shandong University – sequence: 5 givenname: Weifang orcidid: 0000-0003-4675-656X surname: Zhang fullname: Zhang, Weifang organization: Shandong University – sequence: 6 givenname: Chunyan surname: Chen fullname: Chen, Chunyan organization: Shandong University – sequence: 7 givenname: Juan surname: Liu fullname: Liu, Juan email: liujuan@sdu.edu.cn organization: Shandong University – sequence: 8 givenname: Weiming orcidid: 0000-0001-6894-8859 surname: Zhao fullname: Zhao, Weiming email: zhaowm@sdu.edu.cn organization: Shandong University |
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Keywords | INPP4B AKT SGK3 cervical cancer |
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References | 2010; 12 2015; 14 2015; 6 2015; 5 2010; 107 2015; 125 1997; 275 2003; 16 1999; 189 2008; 1 2011; 19 2016; 35 2014; 134 2016; 140 2010; 23 2006; 208 2016; 2 2014; 506 2017; 36 2010; 28 2011; 71 2004; 78 2015; 21 2009; 384 2006; 281 2009; 16 2014; 56 2011; 122 |
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Snippet | Cervical cancer continues to be among the most frequent gynaecologic cancers worldwide. The phosphoinositide 3‐kinase (PI3K)/protein kinase B (AKT) pathway is... Cervical cancer continues to be among the most frequent gynaecologic cancers worldwide. The phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT) pathway is... Cervical cancer continues to be among the most frequent gynaecologic cancers worldwide. The phosphoinositide 3‐kinase ( PI 3K)/protein kinase B ( AKT ) pathway... |
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SubjectTerms | AKT Cell Line, Tumor Cell Movement Cell Proliferation cervical cancer Humans Immediate-Early Proteins - metabolism INPP4B Neoplasm Metastasis Original Phosphoric Monoester Hydrolases - metabolism Phosphorylation Protein-Serine-Threonine Kinases - metabolism Proto-Oncogene Proteins c-akt - metabolism SGK3 Signal Transduction |
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Title | INPP4B restrains cell proliferation and metastasis via regulation of the PI3K/AKT/SGK pathway |
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