Targeting LRRC15 inhibits metastatic dissemination of ovarian cancer.
Upasana RayDeok-Beom JungLing JinYinan XiaoSubramanyam DasariSayantani Sarkar BhattacharyaPrabhu ThirusanguJulie K StaubDebarshi RoyBhaskar RoyS John WerohaXiaonan HouJames W PurcellJamie N Bakkum-GamezScott H KaufmannNagarajan KannanAnirban K MitraViji ShridharPublished in: Cancer research (2021)
Dissemination of ovarian cancer (OC) cells can lead to inoperable metastatic lesions in the bowel and omentum that cause patient death. Here we show that LRRC15, a type-I 15-leucine-rich repeat-containing membrane protein, highly overexpressed in OC bowel metastases compared to matched primary tumors and acts as a potent promoter of omental metastasis. Complementary models of OC demonstrated that LRRC15 expression leads to inhibition of anoikis-induced cell death and promotes adhesion and invasion through matrices that mimic omentum. Mechanistically, LRRC15 interacted with β1-integrin to stimulate activation of focal adhesion kinase (FAK) signaling. As a therapeutic proof of concept, targeting LRRC15 with the specific antibody-drug conjugate ABBV-085 in both early and late metastatic OC cell line xenograft models prevented metastatic dissemination, and these results were corroborated in metastatic patient-derived OC xenograft models. Furthermore, treatment of 3D-spheroid cultures of LRRC15-positive patient-derived ascites with ABBV-085 reduced cell viability. Overall, these data uncover a role for LRRC15 in promoting OC metastasis and suggest a novel and promising therapy to target OC metastases.
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