Abstract
Esophageal squamous cell carcinoma (ESCC) is a very common malignant tumor with poor prognosis in China. Chemokines secreted by tumors are pivotal for the accumulation of CD8++ T lymphocytes within malignant lesions in several types of cancers, but the exact mechanism underlying CD8++ T lymphocyte homing is still unknown in ESCC. In this study, we revealed that, compared with marginal tissues, the expression of both chemokine (C-C motif) ligand 5 (CCL5) and (C-X-C motif) ligand 10 (CXCL10) was upregulated in ESCC tissues. CCL5 expression was positively associated with the overall survival of patients. Meanwhile, RT-PCR data showed that the expression of CCL5 and CXCL10 was positively correlated with the local expressions of the CD8++ T lymphocyte markers (CD8+ and Granzyme B) in tumor tissues. Correspondingly, CD8++ T lymphocytes were more frequently CCR5- and CXCR3- positive in tumor than in peripheral blood. Transwell analysis showed both CCL5 and CXCL10 were important for the chemotactic movement of CD8++ T lymphocytes. Our data indicate that CCL5 and CXCL10 serve as the key chemokines to recruit CD8++ T lymphocytes into ESCC tissue and may play a role in patient survival.
Original language | English (US) |
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Pages (from-to) | 24978-24989 |
Number of pages | 12 |
Journal | Oncotarget |
Volume | 6 |
Issue number | 28 |
DOIs | |
State | Published - 2015 |
Keywords
- CCL5
- CXCL10
- Chemotaxis
- Esophageal squamous cell carcinoma
- T lymphocyte
ASJC Scopus subject areas
- Oncology