open access: Small cell ovarian carcinoma: genomic stability and responsiveness to therapeutics (in mice) Ovarian Cancer and Us OVARIAN CANCER and US Ovarian Cancer and Us

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Thursday, February 21, 2013

open access: Small cell ovarian carcinoma: genomic stability and responsiveness to therapeutics (in mice)



Orphanet Journal of Rare Diseases

Abstract (provisional)

Background

The biology of small cell ovarian carcinoma of the hypercalcemic type (SCCOHT), which is a rare and aggressive form of ovarian cancer, is poorly understood. Tumourigenicity, in vitro growth characteristics, genetic and genomic anomalies, and sensitivity to standard and novel chemotherapeutic treatments were investigated in the unique SCCOHT cell line, BIN-67, to provide further insight in the biology of this rare type of ovarian cancer.

Conclusions

These results show that SCCOHT differs from high-grade serous carcinomas by exhibiting few chromosomal anomalies and lacking TP53 mutations. Although BIN-67 cells are resistant to standard chemotherapeutic agents, their sensitivity to oncolytic viruses suggests that their therapeutic use in SCCOHT should be considered.

The complete article is available as a provisional PDF. The fully formatted PDF and HTML versions are in production.

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