The CD200-CD200R Axis Promotes Squamous Cell Carcinoma Metastasis via Regulation of Cathepsin K.
Iasha Z Khan, Christina A Del Guzzo, Anqi Shao, Jiyoon Cho, Rong Du, Adrienne O Cohen, David M Owens
Author Information
Iasha Z Khan: Department of Dermatology, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, New York, New York.
Christina A Del Guzzo: Department of Dermatology, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, New York, New York.
Anqi Shao: Department of Dermatology, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, New York, New York.
Jiyoon Cho: Department of Dermatology, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, New York, New York.
Rong Du: Department of Dermatology, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, New York, New York.
Adrienne O Cohen: Department of Dermatology, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, New York, New York.
David M Owens: Department of Dermatology, Columbia University Irving Medical Center, Vagelos College of Physicians and Surgeons, New York, New York. do2112@columbia.edu. ORCID
The CD200-CD200R immunoregulatory signaling axis plays an etiologic role in the survival and spread of numerous cancers, primarily through suppression of antitumor immune surveillance. Our previous work outlined a prometastatic role for the CD200-CD200R axis in cutaneous squamous cell carcinoma (cSCC) that is independent of direct T-cell suppression but modulates the function of infiltrating myeloid cells. To identify effectors of the CD200-CD200R axis important for cSCC metastasis, we conducted RNA sequencing profiling of infiltrating CD11BCd200R cells isolated from CD200 versus CD200-null cSCCs and identified the cysteine protease cathepsin K (Ctsk) to be highly upregulated in CD200 cSCCs. CD11BCd200R cells expressed phenotypic markers associated with myeloid-derived suppressor cell-like cells and tumor-associated macrophages and were the primary source of Ctsk expression in cSCC. A Cd200R myeloid cell-cSCC coculture system showed that induction of Ctsk was dependent on engagement of the CD200-CD200R axis, indicating that Ctsk is a target gene of this pathway in the cSCC tumor microenvironment. Inhibition of Ctsk, but not matrix metalloproteinases, significantly blocked cSCC cell migration . Finally, targeted CD200 disruption in tumor cells and Ctsk pharmacologic inhibition significantly reduced cSCC metastasis . Collectively, these findings support the conclusion that CD200 stimulates cSCC invasion and metastasis via induction of Ctsk in CD200R infiltrating myeloid cells. SIGNIFICANCE: These findings highlight the relationship between CD200-CD200R and cathepsin K in cutaneous squamous cell carcinoma metastasis and suggest that either of these components may serve as a viable therapeutic target in this disease.
