4.3 Article

Local production of the chemokines CCL5 and CXCL10 attracts CD8+ T lymphocytes into esophageal squamous cell carcinoma

期刊

ONCOTARGET
卷 6, 期 28, 页码 24978-24989

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.4617

关键词

esophageal squamous cell carcinoma; T lymphocyte; chemotaxis; CCL5; CXCL10

资金

  1. China-US (NFSC-NIH) Program for Biomedical Collaborative Research [812111102]
  2. National Natural Science Foundation of China [81171986]
  3. Ministry of Public Health [20110110001]
  4. Basic and Advanced Technology Research Foundation from Science and Technology Department of Henan Province [112300410153, 122300410155]

向作者/读者索取更多资源

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.

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