Evidence map›Paper›PMID 38916900›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2024

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

Allan M Johansen, Steven D Forsythe, Callum T McGrath, Grayson Barker, Hugo Jimenez, Ravi K Paluri, Boris C Pasche

Abstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Allan M JohansenDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina.ORCID 0000-0002-2896-1749
Steven D ForsytheNeuroendocrine Therapy Section, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.ORCID 0000-0003-4099-6642
Callum T McGrathDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina.ORCID 0009-0003-1509-5997
Grayson BarkerDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina.ORCID 0000-0001-5493-4229
Hugo JimenezKarmanos Cancer Institute, Wayne State University, Detroit, Michigan.ORCID 0000-0002-4234-7075
Ravi K PaluriSection of Hematology/Oncology, Wake Forest School of Medicine, Winston-Salem, North Carolina.ORCID 0000-0002-2317-7082
Boris C PascheKarmanos Cancer Institute, Wayne State University, Detroit, Michigan.ORCID 0000-0002-3750-7898

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
TGF-beta polymorphisms and breast cancer in familiesR01CA112520 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PASCHE, BORIS · 2005 to 2013
$2.1M
TGFBR1 Signaling in Colorectal CancerR01CA137000 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PASCHE, BORIS · 2010 to 2014
$1.5M
TGF-beta pathway polymorphisms and colon cancer riskR01CA108741 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PASCHE, BORIS · 2006 to 2008
$804k
National Cancer Institute (NCI) CA137000NCI NIH HHS P30 CA012197NCI NIH HHS P30 CA022453NCI NIH HHS R01 CA108741NCI NIH HHS R01 CA112520NCI NIH HHS R01 CA137000
6 · The paper itself

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.

Indexed as

Colorectal NeoplasmsDrug Resistance, NeoplasmPancreatic NeoplasmsSignal TransductionTransforming Growth Factor betaAnimalsHumansImmunotherapyTumor MicroenvironmentTransforming Growth Factor beta

Identifiers

PMID38916900
PMCPMC11371528

What Socratic holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.