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| 18 June 1998, Volume 16, Number 24, Pages 3143-3149 |
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| Article |
| Frequent downregulation of the KAI1(CD82) metastasis suppressor protein in human cancer cell lines |
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| A White, P W Lamb and J C Barretta |
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Laboratory of Molecular Carcinogenesis, National Institute of Environmental Health Sciences, National Institutes of Health, POB 12233, Research Triangle Park, North Carolina 27709, USA
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aAuthor for correspondence |
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| Abstract |
 | KAI1 is a metastasis suppressor gene on human chromosome 11p11.2 that encodes a glycoprotein of the transmembrane four superfamily. Reduced KAI1 expression associates with malignant progression of human prostatic, lung and pancreatic cancers, but the role of KAI1 protein in the malignant progression of other human cancers remains to be elucidated. We analysed KAI1 protein in normal and cancer cells of the prostate, ovary, bladder, endometrium, lung and melanocytes by Western blot to determine if KAI1 may be involved in multiple cancers. We also investigated the relationship of KAI1 expression and two other transmembrane four superfamily proteins, CD81 and CD9, in the cells. We found that KAI1 protein was downregulated in 31/42 of the cancer cell lines analysed. Alternatively, some ovarian, bladder and endometrial cells had distinct, heterogeneous KAI1 protein band patterns in Western blots that were due primarily to N-linked glycosylation. Most of the cancer cells expressed two other transmembrane four superfamily proteins, CD81 and CD9. Downregulation of KAI1 protein may be an indicator of metastatic potential in cancers of urogenital, gynecological, and pulmonary origin and in melanomas. KAI1 may also have post-translational modifications specific to tissue type or malignant progression. |
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| Keywords |
 | KAI1 (CD82); metastasis suppressor gene; prostate cancer; transmembrane four superfamily |
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| Received 28 August 1997; revised 20 January 1998; accepted 21 January 1998 |
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| 18 June 1998, Volume 16, Number 24, Pages 3143-3149 |
| Table of contents Previous Abstract Next Article PDF |
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