1. Anaplastic Lymphoma Kinase in Cutaneous Malignancies
- Author
-
Severine Cao and Vinod E. Nambudiri
- Subjects
0301 basic medicine ,Cancer Research ,Pathology ,medicine.medical_specialty ,Review ,lcsh:RC254-282 ,Receptor tyrosine kinase ,03 medical and health sciences ,0302 clinical medicine ,hemic and lymphatic diseases ,medicine ,Anaplastic lymphoma kinase ,Basal cell carcinoma ,Anaplastic large-cell lymphoma ,crizotinib ,Crizotinib ,biology ,business.industry ,Merkel cell carcinoma ,Melanoma ,anaplastic lymphoma kinase ,medicine.disease ,lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,Lymphoma ,030104 developmental biology ,Oncology ,anaplastic large cell lymphoma ,030220 oncology & carcinogenesis ,Cancer research ,biology.protein ,cutaneous malignancy ,business ,medicine.drug - Abstract
Anaplastic lymphoma kinase (ALK) is a receptor tyrosine kinase that has been implicated in the pathogenesis of a variety of neoplasms. As suggested by its name, ALK was first described as part of a translocation product in cases of anaplastic large-cell lymphoma, with other genetic and cytogenetic ALK mutations subsequently coming to attention in the development of many other hematologic and solid organ malignancies. ALK has now been shown to play a role in the pathogenesis of several cutaneous malignancies, including secondary cutaneous systemic anaplastic large-cell lymphoma (ALCL) and primary cutaneous ALCL, melanoma, spitzoid tumors, epithelioid fibrous histiocytoma, Merkel cell carcinoma, and basal cell carcinoma. The characterization of ALK-positivity in these cutaneous malignancies presents exciting opportunities for utilizing ALK-targeted inhibitors in the treatment of these diseases.
- Published
- 2017