4.6 Article

Research Strategies for Low-Survival Cancers

Journal

CANCERS
Volume 13, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/cancers13030528

Keywords

low survival cancer; immuno-oncology; insulin signaling; chromatin re-modelling; transforming growth factor-beta signaling

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The report provides an overview of research presented at the 56th annual conference of the Irish Association for Cancer Research, focusing on low-survival cancers. It emphasizes the need for new and improved treatment strategies for these challenging cancers, highlighting ongoing research efforts aimed at improving patient outcomes.
Simple Summary The Irish Association for Cancer Research (IACR) held its 56th annual conference from 26-28 February 2020, in Galway, Ireland. This report provides a summary overview of the work presented at the conference, which had a particular focus on low-survival cancers. There is a clinical need for new and improved treatment strategies for low-survival cancers. Dynamic and insightful pre-clinical research programs are a critical component in addressing this need, but challenges exist. This manuscript reports on the novel research strategies currently being investigated to improve outcomes for patients with poor prognosis cancers. While substantial progress has been made to improve the diagnosis, prognosis, and survivorship of patients with cancer, certain cancer types, along with metastatic and refractory disease, remain clinical challenges. To improve patient outcomes, ultimately, the cancer research community must meet and overcome these challenges, leading to improved approaches to treat the most difficult cancers. Here, we discuss research progress aimed at gaining a better understanding of the molecular and cellular changes in tumor cells and the surrounding stroma, presented at the 56th Irish Association for Cancer Research (IACR) Annual Conference. With a focus on poor prognosis cancers, such as esophageal and chemo-resistant colorectal cancers, we highlight how detailed molecular knowledge of tumor and stromal biology can provide windows of opportunity for biomarker discovery and therapeutic targets. Even with previously characterized targets, such as phosphoinositide 3-kinase (PI3K), one of the most altered proteins in all human cancers, new insights into how this protein may be more effectively inhibited through novel combination therapies is presented.

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