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The biological role of the CXCL12/CXCR4 axis in esophageal squamous cell carcinoma

期刊

CANCER BIOLOGY & MEDICINE
卷 18, 期 2, 页码 401-410

出版社

CHINA ANTI-CANCER ASSOC
DOI: 10.20892/j.issn.2095-3941.2020.0140

关键词

Esophageal squamous cell carcinoma; C-X-C motif chemokine ligand 12; CXC chemokine receptor 4; antagonists; imaging agent

资金

  1. National Natural Science Foundation of China [81772619, 81702405]
  2. Wu Jieping Medical Foundation [320.6750.17519]
  3. Bethune Charitable Foundation [HZB-2019052818]
  4. Tianjin Natural Science Foundation for Youth [19JCQNJC10800]

向作者/读者索取更多资源

Esophageal squamous cell carcinoma is the main type of esophageal cancer, where abnormal expression of CXCL12 and CXCR4 contributes to tumor proliferation, distant metastases, and worsening prognosis. Antagonists and imaging agents targeting CXCL12/CXCR4 have been developed to interfere with and monitor tumor metastasis.
Esophageal cancer is the eighth most common malignant tumor and the sixth leading cause of cancer related death worldwide. Esophageal squamous cell carcinoma (ESCC) is the main histological type of esophageal cancer, and accounts for 90% of all cancer cases. Despite the progress made in surgery, chemotherapy, and radiotherapy, the mortality rate from esophageal cancer remains high, and the overall 5-year survival rate is less than 20%, even in developed countries. The C-X-C motif chemokine ligand 12 (CXCL12) is a member of the CXC chemokine subgroup, which is widely expressed in a variety of tissues and cells. CXCL12 participates in the regulation of many physiological and pathological processes by binding to its specific receptor, C-X-C motif chemokine receptor type 4 (CXCR4), where it causes embryonic development, immune response, and angiogenesis. In addition, increasing evidence indicates that the CXCL12/CXCR4 axis plays an important role in the biological processes of tumor cells. Studies have shown that CXCL12 and its receptor, CXCR4, are highly expressed in ESCC. This abnormal expression contributes to tumor proliferation, lymph node and distant metastases, and worsening prognosis. At present, antagonists and imaging agents against CXCL12 or CXCR4 have been developed to interfere with the malignant process and monitor metastasis of tumors. This article summarizes the structure, function, and regulatory mechanism of CXCL12/CXCR4 and its role in the malignancy of ESCC. Current results from preclinical research targeting CXCL12/CXCR4 are also summarized to provide a reference for the clinical diagnosis and treatment of ESCC.

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