TGFβ in Pancreas and Colorectal Cancer: Opportunities to Overcome Therapeutic Resistance

Author:

Johansen Allan M.1ORCID,Forsythe Steven D.2ORCID,McGrath Callum T.1ORCID,Barker Grayson13ORCID,Jimenez Hugo3ORCID,Paluri Ravi K.4ORCID,Pasche Boris C.3ORCID

Affiliation:

1. Department of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina. 1

2. Neuroendocrine Therapy Section, National Cancer Institute, National Institutes of Health, Bethesda, Maryland. 2

3. Karmanos Cancer Institute, Wayne State University, Detroit, Michigan. 3

4. Section of Hematology/Oncology, Wake Forest School of Medicine, Winston-Salem, North Carolina. 4

Abstract

Abstract TGFβ is a pleiotropic signaling pathway that plays a pivotal role in regulating a multitude of cellular functions. TGFβ has a dual role in cell regulation where it induces growth inhibition and cell death; however, it can switch to a growth-promoting state under cancerous conditions. TGFβ is upregulated in colorectal cancer and pancreatic cancer, altering the tumor microenvironment and immune system and promoting a mesenchymal state. The upregulation of TGFβ in certain cancers leads to resistance to immunotherapy, and attempts to inhibit TGFβ expression have led to reduced therapeutic resistance when combined with chemotherapy and immunotherapy. Here, we review the current TGFβ inhibitor drugs in clinical trials for pancreatic and colorectal cancer, with the goal of uncovering advances in improving clinical efficacy for TGFβ combinational treatments in patients. Furthermore, we discuss the relevance of alterations in TGFβ signaling and germline variants in the context of personalizing treatment for patients who show lack of response to current therapeutics.

Funder

National Cancer Institute

Publisher

American Association for Cancer Research (AACR)

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