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Establishment and characterization of a human prostatic carcinoma cell line (PC-3).

M E Kaighn, +4 more
- 01 Jul 1979 - 
- Vol. 17, Iss: 1, pp 16-23
TLDR
The establishment, characterization, and tumorigenicity of a new epithelial cell line (PC-3) from a human prostatic adenocarcinoma metastatic to bone is reported, which should be useful in investigating the biochemical changes in advanced prostatic cancer cells and in assessing their response to chemotherapeutic agents.
Abstract
The establishment, characterization, and tumorigenicity of a new epithelial cell line (PC-3) from a human prostatic adenocarcinoma metastatic to bone is reported The cultured cells show anchorage-independent growth in both monolayers and in soft agar suspension and produce subcutaneous tumors in nude mice Culture of the transplanted tumor yielded a human cell line with characteristics identical to those used initially to produce the tumor PC-3 has a greatly reduced dependence upon serum for growth when compared to normal prostatic epithelial cells and does not respond to androgens, glucocorticoids, or epidermal or fibroblast gowth factors Karyotypic analysis by quinacrine banding revealed the cells to be completely aneuploid with a modal chromosome number in the hypotriploid range At least 10 distinctive marker chromosomes were identified The overall karyotype as well as the marker chromosomes are distinct from those of the HeLa cell Electron microscopic studies revealed many features common to neoplastic cells of epithelial origin including numerous microvilli, junctional complexes, abnormal nuclei and nucleoli, abnormal mitochondria, annulate lamellae, and lipoidal bodies Overall, the functional and morphologic characteristics of PC-3 are those of a poorly-differentiated adenocarcinoma These cells should be useful in investigating the biochemical changes in advanced prostatic cancer cells and in assessing their response to chemotherapeutic agents

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Two different forms of p53 localized differently within cells of urogenital tumours.

TL;DR: These findings demonstrate an unusual subcellular localization pattern of p53 in prostate and bladder cancer cells which may indicate another mechanism of inactivation of p 53.
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Autonomous Hedgehog signalling is undetectable in PC-3 prostate cancer cells.

TL;DR: No evidence of autonomous Hedgehog signalling in PC-3 cells is found, irrespective of passage number, and manipulations that should either increase or decrease Hedgehog pathway activity had no effect on reporter activity, and cyclopamine treatment did not affectPC-3 cell viability.
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Diet-induced hyperinsulinemia accelerates growth of androgen-independent PC-3 cells in vitro.

TL;DR: The results provide support for the concept that diet-associated elevation in insulin level may augment the growth of prostate cancer cells through the growth promoting effect of insulin in the androgen-independent prostate cancer PC-3 cells.
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Chromosome 18 suppresses prostate cancer metastases.

TL;DR: The introduction of chromosome 18 significantly reduced tumor burden in extraskeletal sites and the ability of hybrids to metastasize to bone after intra-cardiac inoculation in a nude mouse model suggest that chromosome 18 has a functional role in CaP to suppress growth and metastases.
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An orally active Amazonian plant extract (BIRM) inhibits prostate cancer growth and metastasis

TL;DR: The plant extract BIRM contains antitumor compounds of Mr ≥3500 with potent antiproliferative activity in vitro and in vivo against prostate cancer cells and was found to be resistant to proteinase and heat.
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