Tim-3 expression in cervical cancer promotes tumor metastasis.
<h4>Background</h4>T cell immunoglobulin mucin-3 (Tim-3) has been identified as a negative regulator of anti-tumor immunity. Recent studies highlight the important role of Tim-3 in the CD8(+) T cell exhaustion that takes place in both human and animal cancer models. However, the nature o...
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oai:doaj.org-article:32955eba1a0f4020a8555c010cd723132021-11-18T08:01:24ZTim-3 expression in cervical cancer promotes tumor metastasis.1932-620310.1371/journal.pone.0053834https://doaj.org/article/32955eba1a0f4020a8555c010cd723132013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23335978/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>T cell immunoglobulin mucin-3 (Tim-3) has been identified as a negative regulator of anti-tumor immunity. Recent studies highlight the important role of Tim-3 in the CD8(+) T cell exhaustion that takes place in both human and animal cancer models. However, the nature of Tim-3 expression in the tumor cell and the mechanism by which it inhibits anti-tumor immunity are unclear. This present study aims to determine Tim-3 is expressed in cervical cancer cells and to evaluate the role of Tim-3 in cervical cancer progression.<h4>Methodology</h4>A total of 85 cervical tissue specimens including 43 human cervical cancer, 22 cervical intraepithelial neoplasia (CIN) and 20 chronic cervicitis were involved. Tim-3 expression in tumor cells was detected and was found to correlate with clinicopathological parameters. Meanwhile, expression of Tim-3 was assessed by RT-PCR, Western Blot and confocal microscopy in cervical cancer cell lines, HeLa and SiHa. The migration and invasion potential of Hela cells was evaluated after inhibiting Tim-3 expression by ADV-antisense Tim-3.<h4>Conclusions</h4>We found that Tim-3 was expressed at a higher level in the clinical cervical cancer cells compared to the CIN and chronic cervicitis controls. We supported this finding by confirming the presence of Tim-3 mRNA and protein in the cervical cell lines. Tim-3 expression in tumor cells correlated with clinicopathological parameters. Patients with high expression of Tim-3 had a significant metastatic potential, advanced cancer grades and shorter overall survival than those with lower expression. Multivariate analysis showed that Tim-3 expression was an independent factor for predicting the prognosis of cervical cancer. Significantly, down-regulating the expression of Tim-3 protein inhibited migration and invasion of Hela cells. Our study suggests that the expression of Tim-3 in tumor cells may be an independent prognostic factor for patients with cervical cancer. Moreover, Tim-3 expression may promote metastatic potential in cervical cancers.Yang CaoXiaoxi ZhouXiaoyuan HuangQinlu LiLili GaoLijun JiangMei HuangJianfeng ZhouPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 1, p e53834 (2013) |
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Medicine R Science Q Yang Cao Xiaoxi Zhou Xiaoyuan Huang Qinlu Li Lili Gao Lijun Jiang Mei Huang Jianfeng Zhou Tim-3 expression in cervical cancer promotes tumor metastasis. |
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<h4>Background</h4>T cell immunoglobulin mucin-3 (Tim-3) has been identified as a negative regulator of anti-tumor immunity. Recent studies highlight the important role of Tim-3 in the CD8(+) T cell exhaustion that takes place in both human and animal cancer models. However, the nature of Tim-3 expression in the tumor cell and the mechanism by which it inhibits anti-tumor immunity are unclear. This present study aims to determine Tim-3 is expressed in cervical cancer cells and to evaluate the role of Tim-3 in cervical cancer progression.<h4>Methodology</h4>A total of 85 cervical tissue specimens including 43 human cervical cancer, 22 cervical intraepithelial neoplasia (CIN) and 20 chronic cervicitis were involved. Tim-3 expression in tumor cells was detected and was found to correlate with clinicopathological parameters. Meanwhile, expression of Tim-3 was assessed by RT-PCR, Western Blot and confocal microscopy in cervical cancer cell lines, HeLa and SiHa. The migration and invasion potential of Hela cells was evaluated after inhibiting Tim-3 expression by ADV-antisense Tim-3.<h4>Conclusions</h4>We found that Tim-3 was expressed at a higher level in the clinical cervical cancer cells compared to the CIN and chronic cervicitis controls. We supported this finding by confirming the presence of Tim-3 mRNA and protein in the cervical cell lines. Tim-3 expression in tumor cells correlated with clinicopathological parameters. Patients with high expression of Tim-3 had a significant metastatic potential, advanced cancer grades and shorter overall survival than those with lower expression. Multivariate analysis showed that Tim-3 expression was an independent factor for predicting the prognosis of cervical cancer. Significantly, down-regulating the expression of Tim-3 protein inhibited migration and invasion of Hela cells. Our study suggests that the expression of Tim-3 in tumor cells may be an independent prognostic factor for patients with cervical cancer. Moreover, Tim-3 expression may promote metastatic potential in cervical cancers. |
format |
article |
author |
Yang Cao Xiaoxi Zhou Xiaoyuan Huang Qinlu Li Lili Gao Lijun Jiang Mei Huang Jianfeng Zhou |
author_facet |
Yang Cao Xiaoxi Zhou Xiaoyuan Huang Qinlu Li Lili Gao Lijun Jiang Mei Huang Jianfeng Zhou |
author_sort |
Yang Cao |
title |
Tim-3 expression in cervical cancer promotes tumor metastasis. |
title_short |
Tim-3 expression in cervical cancer promotes tumor metastasis. |
title_full |
Tim-3 expression in cervical cancer promotes tumor metastasis. |
title_fullStr |
Tim-3 expression in cervical cancer promotes tumor metastasis. |
title_full_unstemmed |
Tim-3 expression in cervical cancer promotes tumor metastasis. |
title_sort |
tim-3 expression in cervical cancer promotes tumor metastasis. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2013 |
url |
https://doaj.org/article/32955eba1a0f4020a8555c010cd72313 |
work_keys_str_mv |
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_version_ |
1718422595882188800 |