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Salle de conférence E2-03, Hôpital du Saint-Sacrement Visioconférence : CHUL, salle J-0157 / HEJ, LOEX, salle R-138 « Investigating the use of inhibitors of MNK1/2 in invasive and metastatic cancer » Pre Sonia del Rincón, Ph.D. Professeur adjointe McGill University Invitée par : Pre Solange Landreville Lundi 25 novembre 2019 IRIS # 2229242 15h00 Résumé de la conférence. The eIF4F complex, a critical regulator of mRNA translation can be viewed as a molecular bridge between upstream oncogenic signaling and downstream protein synthesis. Although inhibitors of eIF4F complex members exist (against eIF4A, eIF4G and eIF4E), our approach to block metastatic disease is to block the activity of MNK1/2, the kinases which phosphorylate eIF4E. We have shown that MNK1/2 inhibitors hold therapeutic promise in breast cancer and melanoma. Our research is focused on understanding the tumor-intrinsic and –extrinsic (in immune cells) effects of MNK1/2 signaling.

Pre Sonia del Rincón, Ph.D. · Visioconférence : CHUL, salle J-0157 / HEJ, LOEX, salle R-138 « Investigating the use of inhibitors of MNK1/2 in invasive and metastatic cancer »

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Page 1: Pre Sonia del Rincón, Ph.D. · Visioconférence : CHUL, salle J-0157 / HEJ, LOEX, salle R-138 « Investigating the use of inhibitors of MNK1/2 in invasive and metastatic cancer »

Salle de conférence E2-03, Hôpital du Saint-Sacrement

Visioconférence : CHUL, salle J-0157 / HEJ, LOEX, salle R-138

« Investigating the use of inhibitors of MNK1/2 in invasive and

metastatic cancer »

Pre Sonia del Rincón, Ph.D. Professeur adjointe McGill University Invitée par : Pre Solange Landreville

Lundi 25 novembre 2019

IRIS # 2229242

15h00

Résumé de la conférence.

The eIF4F complex, a critical regulator of mRNA translation can be viewed as a molecular bridge between upstream oncogenic signaling and downstream protein synthesis. Although inhibitors of eIF4F complex members exist (against eIF4A, eIF4G and eIF4E), our approach to block metastatic disease is to block the activity of MNK1/2, the kinases which phosphorylate eIF4E. We have shown that MNK1/2 inhibitors hold therapeutic promise in breast cancer and melanoma. Our research is focused on understanding the tumor-intrinsic and –extrinsic (in immune cells) effects of MNK1/2 signaling.