STGC3 inhibits xenograft tumor growth of nasopharyngeal carcinoma cells by altering the expression of proteins associated with apoptosis
STGC3 is a potential tumor suppressor that inhibits the growth of the nasopharyngeal carcinoma cell line CNE2; the expression of this protein is reduced in nasopharyngeal carcinoma compared with normal nasopharyngeal tissue. In this study, we investigated the tumor-suppressing activity of STGC3 in n...
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Published in | Genetics and molecular biology Vol. 35; no. 1; pp. 18 - 26 |
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Abstract | STGC3 is a potential tumor suppressor that inhibits the growth of the nasopharyngeal carcinoma cell line CNE2; the expression of this protein is reduced in nasopharyngeal carcinoma compared with normal nasopharyngeal tissue. In this study, we investigated the tumor-suppressing activity of STGC3 in nude mice injected subcutaneously with Tet/pTRE-STGC3/CNE2 cells. STGC3 expression was induced by the intraperitoneal injection of doxycycline (Dox). The volume mean of Tet/pTRE-STGC3/CNE2+Dox xenografts was smaller than that of Tet/pTRE/CNE2+Dox xenografts. In addition, Tet/pTRE-STGC3/CNE2+Dox xenografts showed an increase in the percentage of apoptotic cells, a decrease in Bcl-2 protein expression and an increase in Bax protein expression. A proteomic approach was used to assess the protein expression profile associated with STGC3-mediated apoptosis. Western blotting confirmed the differential up-regulation of prohibitin seen in proteomic analysis. These results indicate that overexpression of STGC3 inhibits xenograft growth in nude mice by enhancing apoptotic cell death through altered expression of apoptosis-related proteins such as Bcl-2, Bax and prohibitin. These data contribute to our understanding of the function of STGC3 in human nasopharyngeal carcinoma and provide new clues for investigating other STGC3-associated tumors. |
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AbstractList | STGC3 is a potential tumor suppressor that inhibits the growth of the nasopharyngeal carcinoma cell line CNE2; the expression of this protein is reduced in nasopharyngeal carcinoma compared with normal nasopharyngeal tissue. In this study, we investigated the tumor-suppressing activity of STGC3 in nude mice injected subcutaneously with Tet/pTRE-
STGC3
/CNE2 cells. STGC3 expression was induced by the intraperitoneal injection of doxycycline (Dox). The volume mean of Tet/pTRE-
STGC3
/CNE2+Dox xenografts was smaller than that of Tet/pTRE/CNE2+Dox xenografts. In addition, Tet/pTRE-
STGC3
/CNE2+Dox xenografts showed an increase in the percentage of apoptotic cells, a decrease in Bcl-2 protein expression and an increase in Bax protein expression. A proteomic approach was used to assess the protein expression profile associated with STGC3-mediated apoptosis. Western blotting confirmed the differential up-regulation of prohibitin seen in proteomic analysis. These results indicate that overexpression of STGC3 inhibits xenograft growth in nude mice by enhancing apoptotic cell death through altered expression of apoptosis-related proteins such as Bcl-2, Bax and prohibitin. These data contribute to our understanding of the function of STGC3 in human nasopharyngeal carcinoma and provide new clues for investigating other STGC3-associated tumors. STGC3 is a potential tumor suppressor that inhibits the growth of the nasopharyngeal carcinoma cell line CNE2; the expression of this protein is reduced in nasopharyngeal carcinoma compared with normal nasopharyngeal tissue. In this study, we investigated the tumor-suppressing activity of STGC3 in nude mice injected subcutaneously with Tet/pTRE-STGC3/CNE2 cells. STGC3 expression was induced by the intraperitoneal injection of doxycycline (Dox). The volume mean of Tet/pTRE-STGC3/CNE2+Dox xenografts was smaller than that of Tet/pTRE/CNE2+Dox xenografts. In addition, Tet/pTRE-STGC3/CNE2+Dox xenografts showed an increase in the percentage of apoptotic cells, a decrease in Bcl-2 protein expression and an increase in Bax protein expression. A proteomic approach was used to assess the protein expression profile associated with STGC3-mediated apoptosis. Western blotting confirmed the differential up-regulation of prohibitin seen in proteomic analysis. These results indicate that overexpression of STGC3 inhibits xenograft growth in nude mice by enhancing apoptotic cell death through altered expression of apoptosis-related proteins such as Bcl-2, Bax and prohibitin. These data contribute to our understanding of the function of STGC3 in human nasopharyngeal carcinoma and provide new clues for investigating other STGC3-associated tumors. |
Author | Long, Zhi-Feng Tang, Guo-Hua He, Xiu-Pei Qiu, Qing-Chao He, Xiu-Sheng Hu, Bo Luo, Qiao Chen, Zhu-Chu |
AuthorAffiliation | 5 Department of Otolaryngology, The First People’s Hospital of Yunnan Province, Kunming, China 3 Cancer Research Institute, Central South University, Changsha, China 1 Cancer Research Institute, University of South China, Hengyang, China 4 Hunan Environment-Biological Polytechnic College, Hengyang, China 2 Department of Medicine, Vanderbilt University, Nashville, USA |
AuthorAffiliation_xml | – name: 4 Hunan Environment-Biological Polytechnic College, Hengyang, China – name: 3 Cancer Research Institute, Central South University, Changsha, China – name: 1 Cancer Research Institute, University of South China, Hengyang, China – name: 2 Department of Medicine, Vanderbilt University, Nashville, USA – name: 5 Department of Otolaryngology, The First People’s Hospital of Yunnan Province, Kunming, China – name: The First People's Hospital of Yunnan Province – name: Vanderbilt University – name: Central South University – name: University of Hong Kong – name: Hunan Environment-Biological Polytechnic College |
Author_xml | – sequence: 1 givenname: Qing-Chao surname: Qiu fullname: Qiu, Qing-Chao organization: Cancer Research Institute, University of South China, Hengyang, China – sequence: 2 givenname: Bo surname: Hu fullname: Hu, Bo – sequence: 3 givenname: Xiu-Pei surname: He fullname: He, Xiu-Pei – sequence: 4 givenname: Qiao surname: Luo fullname: Luo, Qiao – sequence: 5 givenname: Guo-Hua surname: Tang fullname: Tang, Guo-Hua – sequence: 6 givenname: Zhi-Feng surname: Long fullname: Long, Zhi-Feng – sequence: 7 givenname: Zhu-Chu surname: Chen fullname: Chen, Zhu-Chu – sequence: 8 givenname: Xiu-Sheng surname: He fullname: He, Xiu-Sheng |
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CitedBy_id | crossref_primary_10_1039_C5TX00391A crossref_primary_10_4238_2012_October_9_9 crossref_primary_10_1111_febs_12838 crossref_primary_10_1080_13102818_2014_916499 |
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Keywords | CNE2 cell line Tet-on nasopharyngeal carcinoma nude mouse two-dimensional electrophoresis STGC3 |
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2009 end-page: 1141 article-title: Cytoskeleton-associated proteins are enriched in human embryonic-stem cell-derived neuroectodermal spheres publication-title: Proteomics contributor: fullname: Chae, JI; Kim, J; Woo, SM; Han, HW; Cho, YK; Oh, KB; Nam, KH; Kang, YK |
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SubjectTerms | BIOCHEMISTRY & MOLECULAR BIOLOGY CNE2 cell line GENETICS & HEREDITY nasopharyngeal carcinoma nude mouse STGC3 Tet-on two-dimensional electrophoresis |
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Title | STGC3 inhibits xenograft tumor growth of nasopharyngeal carcinoma cells by altering the expression of proteins associated with apoptosis |
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