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 inJournal of cellular and molecular medicine Vol. 22; no. 5; pp. 2935 - 2943
Main Authors Chen, Ying, Sun, Zeyu, Qi, Mei, Wang, Xiao, Zhang, Weifang, Chen, Chunyan, Liu, Juan, Zhao, Weiming
Format Journal Article
LanguageEnglish
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.
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
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Issue 5
Keywords INPP4B
AKT
SGK3
cervical cancer
Language English
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2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.
This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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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
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjcmm.13595
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