Role of IKKα in skin squamous cell carcinomas

Author:

Park Eunmi1,Liu Bigang2,Xia Xiaojun3,Zhu Feng2,Jami Willette-Brown4,Hu Yinling

Affiliation:

1. Department of Radiation Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA

2. Department of Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, TX 78957, USA

3. Center for Cell & Gene Therapy, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA

4. Cancer & Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institute of Health, Frederick, MD 21701, USA

Abstract

Squamous cell carcinoma (SCC) and basal cell carcinoma (BCC) are two major types of skin cancer derived from keratinocytes. SCC is a more aggressive type of cancer than BCC in humans. One significant difference between SCC and BCC is that SCC development is generally associated with cell dedifferentiation and morphological changes. When SCC is converted to spindle cell carcinoma, the latest stage of cancer, the tumor cells change to a fibroblastic cell morphology (epithelial-to-mesenchymal transition) and lose their differentiation markers. Recently, several laboratories have reported altered IκB kinase α (IKKα) protein localization, downregulated IKKα, and IKKα gene deletions and mutations in human SCCs of the skin, lung, esophagus, and neck and head. In addition, IKKα reduction promotes chemical carcinogen- and ultraviolet B-induced skin carcinogenesis, and IKKα deletion in keratinocytes causes spontaneous skin SCCs, but not BCCs, in mice. Thus, IKKα emerges as a bona fide skin tumor suppressor. In this article, we will discuss the role of IKKα in skin SCC development.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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