Osteopontin -- a promising biomarker for cancer therapy

被引:123
作者
Wei, Ran [1 ]
Wong, Janet Pik Ching [1 ]
Kwok, Hang Fai [1 ]
机构
[1] Univ Macau, Fac Hlth Sci, Ave Univ, Taipa, Macao, Peoples R China
来源
JOURNAL OF CANCER | 2017年 / 8卷 / 12期
关键词
Angiogenesis; Biomarker; Osteopontin; Therapeutic target; Tumor biology; TUMOR-ASSOCIATED MACROPHAGES; BREAST-CANCER; HEPATOCELLULAR-CARCINOMA; GROWTH-FACTOR; TRANSCRIPTIONAL REGULATION; INHIBITS OSTEOPONTIN; PARATHYROID-HORMONE; CURATIVE RESECTION; BONE SIALOPROTEIN; SIGNALING PATHWAY;
D O I
10.7150/jca.20480
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteopontin (OPN), a multifunctional protein, has emerged as a potentially valuable biomarker for diagnosing and treating cancers. Recent research focuses on its involvement in tumor biology including the cell proliferation, survival, angiogenesis, invasion, and metastasis. Understanding the molecular mechanisms and pharmacological effects of OPN in cancer development could lead to new targets for improving cancer diagnosis and treatment. This review explains how the structurally conserved domains of OPN are associated with OPN signaling mediators and CD44, and how the conserved OPN domains determine biological functions. The authors have reviewed representative works of OPN expression in breast cancer and colorectal cancer to elucidate the relationship between OPN and cancer/tumor biology. It has also been shown that the prognostic sensitivity in non-small cell lung cancer, hepatocellular carcinoma, gastric cancer, and ovarian cancer improved compared to the individual marker when OPN was analyzed in conjunction with other markers. The therapeutic approaches based on OPN inhibitors are discussed to illustrate recent research progress. Previous clinical data has indicated that OPN has played a unique role in cancer development, but further investigation is required to understand the underlying mechanism. More clinical trials are also required to examine the applicability and efficacy of OPN inhibitors in cancer therapy.
引用
收藏
页码:2173 / 2183
页数:11
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