ArticleThe American journal of pathology2001
KAI1 metastasis suppressor gene is frequently down-regulated in cervical carcinoma.
Article in The American journal of pathology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
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21 citing papers in PubMed, 49 citations in OpenAlex.
- Role of a metastatic suppressor gene KAI1/CD82 in the diagnosis and prognosis of breast cancer.Saudi journal of biological sciences · 2021Review
- Gene expression analysis of human prostate cell lines with and without tumor metastasis suppressor CD82.BMC cancer · 2020Article
- EpCAM-claudin-tetraspanin-modulated ovarian cancer progression and drug resistance.Cell adhesion & migration · 2020Article
- Investigations of a Possible Role of SNPs in KAI1 Gene on Its Down-Regulation in Breast Cancer.Asian Pacific journal of cancer prevention : APJCP · 2020Article
- Differential tumor biological role of the tumor suppressor KAI1 and its splice variant in human breast cancer cells.Oncotarget · 2018Article
- Nm23-H1 was involved in regulation of KAI1 expression in high-metastatic lung cancer cells L9981.Journal of thoracic disease · 2016Article
- The novel function of CD82 and its impact on BCL2L12 via AKT/STAT5 signal pathway in acute myelogenous leukemia cells.Leukemia · 2015Article
- ΔNp63α activates CD82 metastasis suppressor to inhibit cancer cell invasion.Cell death & disease · 2014Article
- Expression of the Metastasis Suppressor KAI1 in Uveal Melanoma.Journal of ophthalmology · 2013Article
- Anti-Apoptotic Signature in Thymic Squamous Cell Carcinomas - Functional Relevance of Anti-Apoptotic BIRC3 Expression in the Thymic Carcinoma Cell Line 1889c.Frontiers in oncology · 2013Article
- Metastasis suppressors and the tumor microenvironment.Seminars in cancer biology · 2011Review
- Metastasis suppressor genes at the interface between the environment and tumor cell growth.International review of cell and molecular biology · 2011Review
- Inhibition of allogeneic T-cell response by Kupffer cells expressing indoleamine 2,3-dioxygenase.World journal of gastroenterology · 2010Article
- Down-regulation of the metastasis suppressor protein KAI1/CD82 correlates with occurrence of metastasis, prognosis and presence of HPV DNA in human penile squamous cell carcinoma.Virchows Archiv : an international journal of pathology · 2008Article
- Metastasis suppressors and their roles in breast carcinoma.Journal of mammary gland biology and neoplasia · 2007Review
- Expression of KAI1 and tenascin, and microvessel density are closely correlated with liver metastasis of gastrointestinal adenocarcinoma.Journal of clinical pathology · 2007Article
- Tetraspanin KAI1/CD82 suppresses invasion by inhibiting integrin-dependent crosstalk with c-Met receptor and Src kinases.Oncogene · 2006Article
- KAI1 gene expression in colonic carcinoma and its clinical significances.World journal of gastroenterology · 2004Article
- Effects of KAI1 gene on growth and invasion of human hepatocellular carcinoma MHCC97-H cells.World journal of gastroenterology · 2004Article
- Effects of KAI1/CD82 on biological behavior of human colorectal carcinoma cell line.World journal of gastroenterology · 2003Article
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8 authors at 3 institutions in 2 countries.
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No grant is acknowledged in the PubMed record.
Abstract
KAI1 is a metastasis suppressor gene located on human chromosome 11p11.2. It belongs to a structurally distinct family of cell surface glycoproteins. Decreased KAI1 expression has been observed in several common solid epithelial tumors, including prostatic, pancreatic, lung, hepatic, colorectal, ovarian, and esophageal cancers. A recent study also observed frequent loss of KAI1 expression in a number of squamous cell carcinomas of the cervix by immunohistochemical technique. To further confirm whether this gene is altered in this malignancy, we analyzed KAI1 expression in various stages of cervical carcinoma by a molecular method. Total cellular RNA was extracted from 84 primary invasive cervical carcinomas and 6 metastatic or recurrent lesions. cDNA was synthesized and was used for real-time quantitative polymerase chain reaction analysis. The level of KAI1 expression was obtained as the value of threshold cycle (Ct) and was quantitated with a comparative Ct method. In addition, paraffin blocks of the tumors were selected and prepared for immunohistochemical study with an anti-KAI1 polyclonal antibody, C-16. Both the real-time quantitative polymerase chain reaction method and immunohistochemical study revealed a frequent decrease in KAI1 expression in invasive cervical cancers and metastatic or recurrent lesions. However, the reduction in KAI1 was not related to progression of the disease. When tumor cell differentiation was analyzed, poorly differentiated tumors showed a greater decrease in KAI1 expression than well or moderately differentiated tumors (P < 0.001). Histologically, KAI1 loss was observed equally in both squamous cell carcinoma and adeno-/adenosquamous carcinoma. Since down-regulation of KAI1 occurs in both early and late stages of cervical cancer, we suggest that its involvement in the progression of this malignancy is an early event.
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