Oncotarget Volume 11, Issue 5: Trop-2 expression was evaluated in 10 formalin-fixed-paraffined-embedded CS by immunohistochemistry and 9 primary CS cell-lines by flow-cytometry.
One Trop-2 low/negative and two Trop-2 positive cell-lines were tested in cell-viability assays.
Trop-2 positive cell-lines showed higher sensitivity to SG in vitro when compared to Trop-2 low/negative cell lines.
Dr. Alessandro D. Santin from the Department of Obstetrics, Gynecology and Reproductive Sciences at Yale University School of Medicine in New Haven Connecticut, USA said in their Oncotarget paper, "Carcinosarcomas (CS), also known as mixed malignant Mullerian tumors (MMMT), account for less than 5% of all gynecologic cancers."
"Carcinosarcomas (CS), also known as mixed malignant Mullerian tumors (MMMT), account for less than 5% of all gynecologic cancers."
- Dr. Alessandro D. Santin, Department of Obstetrics, Gynecology and Reproductive Sciences at Yale University School of Medicine
Non-cleavable linkers manifest anti-tumor activity only after internalization while ADCs with cleavable linkers can kill not only the antigen-positive target cells but also the surrounding antigen-negative cells and they, therefore, are more suitable for the treatment of tumors with heterogeneous antigen expression.
Notably, Trop-2 is highly expressed on the surface of many epithelial tumors when compared to normal cells, and this feature makes Trop-2 an excellent target for ADCs.
Trop-2 overexpression among uterine cancers has been previously reported as high as 96% in endometrioid endometrial cancers and 65% in uterine serous carcinoma.
Recently, there have been multiple clinical trials in a variety of advanced solid cancers including breast, urothelial cancer, small cell lung cancer and non-small cell lung cancer that have shown encouraging the therapeutic activity of SG.
The objective of this study was to evaluate the expression of Trop-2 in CS tissues and primary CS cell lines and to examine the preclinical anti-tumor activity of SG in vitro and in vivo against multiple primary CS models and xenografts.
The Yale Research Team concluded that the results of their Oncotarget paper demonstrate,
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Full text - https://doi.org/10.18632/oncotarget.27342
Correspondence to - Alessandro D. Santin - alessandro.santin@yale.edu
Keywords - sacituzumab govitecan, IMMU-132, uterine carcinosarcoma, trop-2
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