Insights into the Role of PAX-3 in the Development of Melanocytes and Melanoma.

Jessica Diann Hathaway, Azizul Haque
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引用次数: 6

Abstract

Melanoma is the deadliest form of skin cancer in the United States with an increasing prevalence. However, the development of melanoma from a melanocyte precursor is still poorly defined. Understanding the molecules responsible for melanoma progression may lead to improved targeted therapy. One potential molecule is the paired box-3 (PAX-3) protein, which has been implicated in the development of melanocytes and malignant melanoma. In melanoma, the expression of PAX-3 is believed to be differentially regulated, and has been linked with malignancies and staging of the disease. The loss of PAX-3 regulation has also been associated with the loss of transforming growth factor-beta (TGF-β) activity, but its effect on PAX-3 in differentiated melanocytes as well as metastatic melanoma remains unclear. Understanding PAX-3 regulation could potentially shift melanoma to a less aggressive and less metastatic disease. This review summarizes our current knowledge on PAX-3 during melanocyte development, its regulation, and its implications in the development of novel chemo-immunotherapeutics against metastatic melanoma.

PAX-3在黑色素细胞和黑色素瘤发展中的作用。
黑色素瘤是美国最致命的皮肤癌,发病率越来越高。然而,黑素细胞前体的黑色素瘤的发展仍然不明确。了解导致黑色素瘤进展的分子可能会改善靶向治疗。一个潜在的分子是配对盒3 (PAX-3)蛋白,它与黑色素细胞和恶性黑色素瘤的发展有关。在黑色素瘤中,PAX-3的表达被认为是受差异调控的,并且与恶性肿瘤和疾病分期有关。PAX-3调控的缺失也与转化生长因子-β (TGF-β)活性的缺失有关,但其在分化黑色素细胞和转移性黑色素瘤中对PAX-3的影响尚不清楚。了解PAX-3调控可能潜在地将黑色素瘤转变为一种侵袭性和转移性较低的疾病。本文综述了目前关于PAX-3在黑色素细胞发育过程中的作用、其调控作用及其在开发新的化学免疫疗法治疗转移性黑色素瘤中的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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