2026-04-17T06:56:57Zhttps://recercat.cat/oai/request

oai:recercat.cat:2445/2223402025-12-04T19:16:36Zcom_2072_1057col_2072_478858col_2072_478916col_2072_478917

00925njm 22002777a 4500 dc Otero Mateo, Marc author Estrany Jr, Francesc author Arcas Márquez, Sabrina author Moya Borrego, Laura author Castellano, Giancarlo author Castany Roma, Miquel author Alemany Bonastre, Ramon author Fillat i Fonts, Cristina author 2025-07-17T12:25:05Z 2025-07-17T12:25:05Z 2025-03-01 2025-05-16T11:55:20Z Oncolytic adenoviral therapy is a promising approach for pancreatic cancer treatment. However, the limited capacity of murine cells to produce infectious viral progeny precludes the full evaluation of the virotherapy in a suitable immunocompetent mouse model. Here, we report that the murine KPC-I cell line, established from pancreatic tumors developed in to adenoviral replication and generates a progeny of infective virions similar to those from infected human A549 cells. A comparative study with the semipermissive murine CMT64.6 cells reveals that adenoviral infection of KPC-I cells substantially increases the release of infective particles, with a correlating enhanced susceptibility to adenovirus-induced autophagy. Remarkably, systemic delivery of the oncolytic adenovirus AdNuPARE1A in athymic mice bearing KPC-I tumors results in significant inhibition of tumor growth. Moreover, KPC-I tumors in immunocompetent mice with intratumoral administration of AdNuPARE1A or ICOVIR15kDelE3 display significant antitumoral effects, with evidence of adenoviral replication. Collectively, our data show that KPC-I cells are permissive to human oncolytic adenovirus replication, rendering KPC-I syngeneic tumors an interesting model to evaluate the multifaceted antitumor activities of oncolytic adenovirus. Càncer de pàncrees Terapèutica Pancreas cancer Therapeutics KPC pancreatic cancer cells are a novel immunocompetent murine model supporting human adenovirus replication and tumor oncolysis