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Functional proteomic analysis reveals the involvement of KIAA1199 in breast cancer growth, motility and invasiveness

BACKGROUND: KIAA1199 is a recently identified novel gene that is up-regulated in human cancer with poor survival. Our proteomic study on signaling polarity in chemotactic cells revealed KIAA1199 as a novel protein target that may be involved in cellular chemotaxis and motility. In the present study,...

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Autores principales: Jami, Mohammad-Saeid, Hou, Jinxuan, Liu, Miao, Varney, Michelle L, Hassan, Hesham, Dong, Jixin, Geng, Liying, Wang, Jing, Yu, Fang, Huang, Xin, Peng, Hong, Fu, Kai, Li, Yan, Singh, Rakesh K, Ding, Shi-Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007601/
https://www.ncbi.nlm.nih.gov/pubmed/24628760
http://dx.doi.org/10.1186/1471-2407-14-194
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author Jami, Mohammad-Saeid
Hou, Jinxuan
Liu, Miao
Varney, Michelle L
Hassan, Hesham
Dong, Jixin
Geng, Liying
Wang, Jing
Yu, Fang
Huang, Xin
Peng, Hong
Fu, Kai
Li, Yan
Singh, Rakesh K
Ding, Shi-Jian
author_facet Jami, Mohammad-Saeid
Hou, Jinxuan
Liu, Miao
Varney, Michelle L
Hassan, Hesham
Dong, Jixin
Geng, Liying
Wang, Jing
Yu, Fang
Huang, Xin
Peng, Hong
Fu, Kai
Li, Yan
Singh, Rakesh K
Ding, Shi-Jian
author_sort Jami, Mohammad-Saeid
collection PubMed
description BACKGROUND: KIAA1199 is a recently identified novel gene that is up-regulated in human cancer with poor survival. Our proteomic study on signaling polarity in chemotactic cells revealed KIAA1199 as a novel protein target that may be involved in cellular chemotaxis and motility. In the present study, we examined the functional significance of KIAA1199 expression in breast cancer growth, motility and invasiveness. METHODS: We validated the previous microarray observation by tissue microarray immunohistochemistry using a TMA slide containing 12 breast tumor tissue cores and 12 corresponding normal tissues. We performed the shRNA-mediated knockdown of KIAA1199 in MDA-MB-231 and HS578T cells to study the role of this protein in cell proliferation, migration and apoptosis in vitro. We studied the effects of KIAA1199 knockdown in vivo in two groups of mice (n = 5). We carried out the SILAC LC-MS/MS based proteomic studies on the involvement of KIAA1199 in breast cancer. RESULTS: KIAA1199 mRNA and protein was significantly overexpressed in breast tumor specimens and cell lines as compared with non-neoplastic breast tissues from large-scale microarray and studies of breast cancer cell lines and tumors. To gain deeper insights into the novel role of KIAA1199 in breast cancer, we modulated KIAA1199 expression using shRNA-mediated knockdown in two breast cancer cell lines (MDA-MB-231 and HS578T), expressing higher levels of KIAA1199. The KIAA1199 knockdown cells showed reduced motility and cell proliferation in vitro. Moreover, when the knockdown cells were injected into the mammary fat pads of female athymic nude mice, there was a significant decrease in tumor incidence and growth. In addition, quantitative proteomic analysis revealed that knockdown of KIAA1199 in breast cancer (MDA-MB-231) cells affected a broad range of cellular functions including apoptosis, metabolism and cell motility. CONCLUSIONS: Our findings indicate that KIAA1199 may play an important role in breast tumor growth and invasiveness, and that it may represent a novel target for biomarker development and a novel therapeutic target for breast cancer.
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spelling pubmed-40076012014-05-03 Functional proteomic analysis reveals the involvement of KIAA1199 in breast cancer growth, motility and invasiveness Jami, Mohammad-Saeid Hou, Jinxuan Liu, Miao Varney, Michelle L Hassan, Hesham Dong, Jixin Geng, Liying Wang, Jing Yu, Fang Huang, Xin Peng, Hong Fu, Kai Li, Yan Singh, Rakesh K Ding, Shi-Jian BMC Cancer Research Article BACKGROUND: KIAA1199 is a recently identified novel gene that is up-regulated in human cancer with poor survival. Our proteomic study on signaling polarity in chemotactic cells revealed KIAA1199 as a novel protein target that may be involved in cellular chemotaxis and motility. In the present study, we examined the functional significance of KIAA1199 expression in breast cancer growth, motility and invasiveness. METHODS: We validated the previous microarray observation by tissue microarray immunohistochemistry using a TMA slide containing 12 breast tumor tissue cores and 12 corresponding normal tissues. We performed the shRNA-mediated knockdown of KIAA1199 in MDA-MB-231 and HS578T cells to study the role of this protein in cell proliferation, migration and apoptosis in vitro. We studied the effects of KIAA1199 knockdown in vivo in two groups of mice (n = 5). We carried out the SILAC LC-MS/MS based proteomic studies on the involvement of KIAA1199 in breast cancer. RESULTS: KIAA1199 mRNA and protein was significantly overexpressed in breast tumor specimens and cell lines as compared with non-neoplastic breast tissues from large-scale microarray and studies of breast cancer cell lines and tumors. To gain deeper insights into the novel role of KIAA1199 in breast cancer, we modulated KIAA1199 expression using shRNA-mediated knockdown in two breast cancer cell lines (MDA-MB-231 and HS578T), expressing higher levels of KIAA1199. The KIAA1199 knockdown cells showed reduced motility and cell proliferation in vitro. Moreover, when the knockdown cells were injected into the mammary fat pads of female athymic nude mice, there was a significant decrease in tumor incidence and growth. In addition, quantitative proteomic analysis revealed that knockdown of KIAA1199 in breast cancer (MDA-MB-231) cells affected a broad range of cellular functions including apoptosis, metabolism and cell motility. CONCLUSIONS: Our findings indicate that KIAA1199 may play an important role in breast tumor growth and invasiveness, and that it may represent a novel target for biomarker development and a novel therapeutic target for breast cancer. BioMed Central 2014-03-15 /pmc/articles/PMC4007601/ /pubmed/24628760 http://dx.doi.org/10.1186/1471-2407-14-194 Text en Copyright © 2014 Jami et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Jami, Mohammad-Saeid
Hou, Jinxuan
Liu, Miao
Varney, Michelle L
Hassan, Hesham
Dong, Jixin
Geng, Liying
Wang, Jing
Yu, Fang
Huang, Xin
Peng, Hong
Fu, Kai
Li, Yan
Singh, Rakesh K
Ding, Shi-Jian
Functional proteomic analysis reveals the involvement of KIAA1199 in breast cancer growth, motility and invasiveness
title Functional proteomic analysis reveals the involvement of KIAA1199 in breast cancer growth, motility and invasiveness
title_full Functional proteomic analysis reveals the involvement of KIAA1199 in breast cancer growth, motility and invasiveness
title_fullStr Functional proteomic analysis reveals the involvement of KIAA1199 in breast cancer growth, motility and invasiveness
title_full_unstemmed Functional proteomic analysis reveals the involvement of KIAA1199 in breast cancer growth, motility and invasiveness
title_short Functional proteomic analysis reveals the involvement of KIAA1199 in breast cancer growth, motility and invasiveness
title_sort functional proteomic analysis reveals the involvement of kiaa1199 in breast cancer growth, motility and invasiveness
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4007601/
https://www.ncbi.nlm.nih.gov/pubmed/24628760
http://dx.doi.org/10.1186/1471-2407-14-194
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