Novel role of VMP1 as modifier of the pancreatic tumor cell response to chemotherapeutic drugs

Marine Gilabert, Maria Inés Vaccaro, Martin E. Fernandez-Zapico, Ezequiel L. Calvo, Olivier Turrini, Véronique Secq, Stéphane Garcia, Vincent Moutardier, Gwen Lomberk, Nelson Dusetti, Raul Urrutia, Juan L. Iovanna

Research output: Contribution to journalArticlepeer-review

9 Scopus citations


We hypothesized that inhibiting molecules that mediate the adaptation response to cellular stress can antagonize the resistance of pancreatic cancer cells to chemotherapeutic drugs. Toward this end, here, we investigated how VMP1, a stress-induced autophagy-associated protein, modulate stress responses triggered by chemotherapeutic agents in PDAC. We find that VMP1 is particularly over-expressed in poorly differentiated human pancreatic cancer. Pharmacological studies show that drugs that work, in part, via the endoplasmic reticulum stress response, induce VMP1 expression. Similarly, VMP1 is induced by known endoplasmic reticulum stress activators. Genetic inactivation of VMP1 using RNAi-based antagonize the pancreatic cancer stress response to antitumoral agents. Functionally, we find that VMP1 regulates both autophagy and chemotherapeutic resistance even in the presence of chloroquin, ATG5 or Beclin 1 siRNAs, or a Beclin 1-binding VMP1 mutant. In addition, VMP1 modulates endoplasmic reticulum stress independently of its coupling to the molecular and cellular autophagy machinery. Preclinical studies demonstrate that xenografts expressing an inducible and tractable form of VMP1 show increased resistance to the gemcitabine treatment. These results underscore a novel role for VMP1 as a potential therapeutic target for combinatorial therapies aimed at sensitizing pancreatic cancer cells to chemotherapeutic agents as well as provide novel molecular mechanisms to better understand this phenomenon.

Original languageEnglish (US)
Pages (from-to)1834-1843
Number of pages10
JournalJournal of Cellular Physiology
Issue number9
StatePublished - Sep 2013

ASJC Scopus subject areas

  • Physiology
  • Clinical Biochemistry
  • Cell Biology


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