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Platinum Chemotherapy Induces Lymphangiogenesis in Cancerous and Healthy Tissues That Can be Prevented With Adjuvant Anti-VEGFR3 Therapy

Authors :
Harris, Alexandra R.
Esparza, Savieay
Azimi, Mohammad S.
Cornelison, Robert
Azar, Francesca N.
Llaneza, Danielle C.
Belanger, Maura
Mathew, Alexander
Tkachenko, Svyatoslav
Perez, Matthew J.
Rosean, Claire Buchta
Bostic, Raegan R.
Cornelison, R. Chase
Tate, Kinsley M.
Peirce-Cottler, Shayn M.
Paquette, Cherie
Mills, Anne
Landen, Charles N.
Saucerman, Jeff
Dillon, Patrick M.
Pompano, Rebecca R.
Rutkowski, Melanie A.
Munson, Jennifer M.
Harris, Alexandra R.
Esparza, Savieay
Azimi, Mohammad S.
Cornelison, Robert
Azar, Francesca N.
Llaneza, Danielle C.
Belanger, Maura
Mathew, Alexander
Tkachenko, Svyatoslav
Perez, Matthew J.
Rosean, Claire Buchta
Bostic, Raegan R.
Cornelison, R. Chase
Tate, Kinsley M.
Peirce-Cottler, Shayn M.
Paquette, Cherie
Mills, Anne
Landen, Charles N.
Saucerman, Jeff
Dillon, Patrick M.
Pompano, Rebecca R.
Rutkowski, Melanie A.
Munson, Jennifer M.
Publication Year :
2022

Abstract

Chemotherapy has been used to inhibit cancer growth for decades, but emerging evidence shows it can affect the tumor stroma, unintentionally promoting cancer malignancy. After treatment of primary tumors, remaining drugs drain via lymphatics. Though all drugs interact with the lymphatics, we know little of their impact on them. Here, we show a previously unknown effect of platinums, a widely used class of chemotherapeutics, to directly induce systemic lymphangiogenesis and activation. These changes are dose-dependent, long-lasting, and occur in healthy and cancerous tissue in multiple mouse models of breast cancer. We found similar effects in human ovarian and breast cancer patients whose treatment regimens included platinums. Carboplatin treatment of healthy mice prior to mammary tumor inoculation increased cancer metastasis as compared to no pre-treatment. These platinum-induced phenomena could be blocked by VEGFR3 inhibition. These findings have implications for cancer patients receiving platinums and may support the inclusion of anti-VEGFR3 therapy into treatment regimens or differential design of treatment regimens to alter these potential effects.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1346846096
Document Type :
Electronic Resource