TSPY potentiates cell proliferation and tumorigenesis by promoting cell cycle progression in HeLa and NIH3T3 cells

<p>Abstract</p> <p>Background</p> <p>TSPY is a repeated gene mapped to the critical region harboring the gonadoblastoma locus on the Y chromosome (GBY), the only oncogenic locus on this male-specific chromosome. Elevated levels of TSPY have been observed in gonadoblasto...

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Main Authors: Chan Wai-Yee, Lee Tin-Lap, Liu Xing, Oram Shane W, Lau Yun-Fai
Format: Article
Language:English
Published: BMC 2006-06-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/6/154
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author Chan Wai-Yee
Lee Tin-Lap
Liu Xing
Oram Shane W
Lau Yun-Fai
author_facet Chan Wai-Yee
Lee Tin-Lap
Liu Xing
Oram Shane W
Lau Yun-Fai
author_sort Chan Wai-Yee
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>TSPY is a repeated gene mapped to the critical region harboring the gonadoblastoma locus on the Y chromosome (GBY), the only oncogenic locus on this male-specific chromosome. Elevated levels of TSPY have been observed in gonadoblastoma specimens and a variety of other tumor tissues, including testicular germ cell tumors, prostate cancer, melanoma, and liver cancer. TSPY contains a SET/NAP domain that is present in a family of cyclin B and/or histone binding proteins represented by the oncoprotein SET and the nucleosome assembly protein 1 (NAP1), involved in cell cycle regulation and replication.</p> <p>Methods</p> <p>To determine a possible cellular function for TSPY, we manipulated the TSPY expression in HeLa and NIH3T3 cells using the Tet-off system. Cell proliferation, colony formation assays and tumor growth in nude mice were utilized to determine the TSPY effects on cell growth and tumorigenesis. Cell cycle analysis and cell synchronization techniques were used to determine cell cycle profiles. Microarray and RT-PCR were used to investigate gene expression in TSPY expressing cells.</p> <p>Results</p> <p>Our findings suggest that TSPY expression increases cell proliferation <it>in vitro </it>and tumorigenesis <it>in vivo</it>. Ectopic expression of TSPY results in a smaller population of the host cells in the G<sub>2</sub>/M phase of the cell cycle. Using cell synchronization techniques, we show that TSPY is capable of mediating a rapid transition of the cells through the G<sub>2</sub>/M phase. Microarray analysis demonstrates that numerous genes involved in the cell cycle and apoptosis are affected by TSPY expression in the HeLa cells.</p> <p>Conclusion</p> <p>These data, taken together, have provided important insights on the probable functions of TSPY in cell cycle progression, cell proliferation, and tumorigenesis.</p>
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spelling doaj.art-73ec03dc45e948688f1e9f2d0921021c2022-12-22T00:57:21ZengBMCBMC Cancer1471-24072006-06-016115410.1186/1471-2407-6-154TSPY potentiates cell proliferation and tumorigenesis by promoting cell cycle progression in HeLa and NIH3T3 cellsChan Wai-YeeLee Tin-LapLiu XingOram Shane WLau Yun-Fai<p>Abstract</p> <p>Background</p> <p>TSPY is a repeated gene mapped to the critical region harboring the gonadoblastoma locus on the Y chromosome (GBY), the only oncogenic locus on this male-specific chromosome. Elevated levels of TSPY have been observed in gonadoblastoma specimens and a variety of other tumor tissues, including testicular germ cell tumors, prostate cancer, melanoma, and liver cancer. TSPY contains a SET/NAP domain that is present in a family of cyclin B and/or histone binding proteins represented by the oncoprotein SET and the nucleosome assembly protein 1 (NAP1), involved in cell cycle regulation and replication.</p> <p>Methods</p> <p>To determine a possible cellular function for TSPY, we manipulated the TSPY expression in HeLa and NIH3T3 cells using the Tet-off system. Cell proliferation, colony formation assays and tumor growth in nude mice were utilized to determine the TSPY effects on cell growth and tumorigenesis. Cell cycle analysis and cell synchronization techniques were used to determine cell cycle profiles. Microarray and RT-PCR were used to investigate gene expression in TSPY expressing cells.</p> <p>Results</p> <p>Our findings suggest that TSPY expression increases cell proliferation <it>in vitro </it>and tumorigenesis <it>in vivo</it>. Ectopic expression of TSPY results in a smaller population of the host cells in the G<sub>2</sub>/M phase of the cell cycle. Using cell synchronization techniques, we show that TSPY is capable of mediating a rapid transition of the cells through the G<sub>2</sub>/M phase. Microarray analysis demonstrates that numerous genes involved in the cell cycle and apoptosis are affected by TSPY expression in the HeLa cells.</p> <p>Conclusion</p> <p>These data, taken together, have provided important insights on the probable functions of TSPY in cell cycle progression, cell proliferation, and tumorigenesis.</p>http://www.biomedcentral.com/1471-2407/6/154
spellingShingle Chan Wai-Yee
Lee Tin-Lap
Liu Xing
Oram Shane W
Lau Yun-Fai
TSPY potentiates cell proliferation and tumorigenesis by promoting cell cycle progression in HeLa and NIH3T3 cells
BMC Cancer
title TSPY potentiates cell proliferation and tumorigenesis by promoting cell cycle progression in HeLa and NIH3T3 cells
title_full TSPY potentiates cell proliferation and tumorigenesis by promoting cell cycle progression in HeLa and NIH3T3 cells
title_fullStr TSPY potentiates cell proliferation and tumorigenesis by promoting cell cycle progression in HeLa and NIH3T3 cells
title_full_unstemmed TSPY potentiates cell proliferation and tumorigenesis by promoting cell cycle progression in HeLa and NIH3T3 cells
title_short TSPY potentiates cell proliferation and tumorigenesis by promoting cell cycle progression in HeLa and NIH3T3 cells
title_sort tspy potentiates cell proliferation and tumorigenesis by promoting cell cycle progression in hela and nih3t3 cells
url http://www.biomedcentral.com/1471-2407/6/154
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