Abstract |
Prostatic small cell carcinoma is an aggressive subtype of prostate cancer that usually appears as a progression of the original adenocarcinoma. We describe here the WISH-PC2, a novel neuroendocrine xenograft of small cell carcinoma of the prostate. This xenograft was established from a poorly differentiated prostate adenocarcinoma and is serially transplanted in immune-compromised mice where it grows within the prostate, liver, and bone, inducing osteolytic lesions with foci of osteoblastic activity. It secretes to the mouse Chromogranin A and expresses prostate plasma carcinoma tumor antigen-1, six-transmembrane epithelial antigen of the prostate, and members of the Erb-B receptor family. It does not express prostate-specific antigen, prostate stem cell antigen, prostate-specific membrane antigen, and androgen receptor, and it grows independently of androgen. Altogether, WISH-PC2 provides an unlimited source in which to study the involvement of neuroendocrine cells in the progression of prostatic adenocarcinoma and can serve as a novel model for the testing of new therapeutic strategies for prostatic small cell carcinoma.
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Authors | J H Pinthus, T Waks, D G Schindler, A Harmelin, J W Said, A Belldegrun, J Ramon, Z Eshhar |
Journal | Cancer research
(Cancer Res)
Vol. 60
Issue 23
Pg. 6563-7
(Dec 01 2000)
ISSN: 0008-5472 [Print] United States |
PMID | 11118033
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
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Topics |
- Adenocarcinoma
(pathology)
- Aged
- Animals
- Carcinoma, Small Cell
(drug therapy, pathology)
- Cell Differentiation
(physiology)
- Cell Division
(physiology)
- Disease Models, Animal
- Humans
- Male
- Mice
- Mice, Inbred BALB C
- Mice, Inbred NOD
- Mice, SCID
- Phenotype
- Prostatic Neoplasms
(drug therapy, pathology)
- Tumor Cells, Cultured
- Xenograft Model Antitumor Assays
(methods)
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