Mutant and Wild-Type RAS Cross-talk and Stoichiometric Deficiencies Are Determinants of Sensitivity to Targeted Therapies in KRASG12R Pancreatic Ductal Adenocarcinoma.
Article in Cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
0numbers the graph read from it
0cells of the map it votes in
4citing 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.
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
27 authors.
Mandana KamgarDivision of Hematology and Oncology, Department of Medicine, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0001-9364-2712
G Aaron HobbsDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, South Carolina.ORCID 0000-0002-4751-9681
Raven DavidsonDepartment of Biochemistry, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0009-0006-3117-5040
Daniel DorbinDepartment of Biochemistry, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0003-2484-7102
Juliannie HerreraDepartment of Biochemistry, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0009-0008-2034-9695
John F LangenheimDepartment of Pharmacology, Physiology, and Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania.ORCID 0000-0001-8222-5286
Rachel A BurgeDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, South Carolina.ORCID 0000-0001-9363-4333
Mohammed AldakkakDepartment of Surgery, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0009-0001-2855-3278
Ryan D ConrardyData Science Institute, Division of Biostatistics, Medical College of Wisconsin, Milwaukee, Wisconsin.ORCID 0000-0002-8019-6909
Aniko SzaboData Science Institute, Division of Biostatistics, Medical College of Wisconsin, Milwaukee, Wisconsin.ORCID 0000-0002-8129-0614
Sam Z ThaljiDepartment of Surgery, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0002-2681-2109
Bradley MayerDepartment of Pharmacy, Froedtert Health, Milwaukee, Wisconsin.ORCID 0009-0009-3995-7858
Justin J GrahlDepartment of Pharmacy, Froedtert Health, Milwaukee, Wisconsin.ORCID 0009-0004-0290-2478
Brian Y ChungCancer Center, Medical College of Wisconsin, Milwaukee, Wisconsin.ORCID 0000-0002-6423-5226
Alexandria PhanDivision of Hematology and Oncology, Department of Medicine, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0002-2953-3033
James P ThomasDivision of Hematology and Oncology, Department of Medicine, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0009-0006-7170-5982
Y David SeoDepartment of Surgery, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0001-6837-5018
Douglas B EvansDepartment of Surgery, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0001-5708-467X
Kathleen K ChristiansDepartment of Surgery, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0001-7566-3819
Beth EricksonDepartment of Radiation Oncology, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0009-0004-8908-5633
William A HallDepartment of Radiation Oncology, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0001-7017-6755
Ben GeorgeDivision of Hematology and Oncology, Department of Medicine, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0002-9667-9833
Susan TsaiDepartment of Surgery, The Ohio State University Wexner Medical Center and James Comprehensive Cancer Center, Columbus, Ohio.ORCID 0000-0003-3685-2451
Nikki K LytleDepartment of Surgery, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0002-9936-4212
Channing J DerDepartment of Pharmacology, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.ORCID 0000-0002-7751-2747
Razelle KurzrockDivision of Hematology and Oncology, Department of Medicine, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0003-4110-1214
Thomas McFallDepartment of Biochemistry, Medical College of Wisconsin and the LaBahn Pancreatic Cancer Program, Milwaukee, Wisconsin.ORCID 0000-0002-5284-6994
Funding
The role of SMAD1 and SATB2 in colon patterningP20GM130457 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI STEPHEN A DUNCAN · 2020 to 2026
$18.7M
Redefining indications of EGFR inhibitors in cancers that harbor mutant RASR01CA276771 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Thomas Bradley McFall · 2024 to 2026
$1.8M
American Cancer Society (ACS) Institutional Research Grant IRG #19-138-34Cancer Center, Medical College of Wisconsin (MCWCC) Byrne Scholar FundConcern Foundation (Concern Foundation Inc.) 2022 Concern Foundation Career Development AwardHollings Cancer Center, Medical University of South Carolina (Hollings Cancer Center) Hollings Cancer Center Abney FellowshipMedical College of Wisconsin (MCW) Department of Surgery We Care FundMedical College of Wisconsin (MCW) Medical College of WisconsinNational Cancer Institute (NCI) 1R01CA276771-01A1National Institute of General Medical Sciences (NIGMS) NIGMS P20 GM130457NCI NIH HHS L30 CA284420NCI NIH HHS R01 CA276771NIGMS NIH HHS P20 GM130457Pancreatic Cancer Action Network (PCAN) Career Development Award in memory of Skip Viragh (22-20-HOBB)
6 · The paper itself
Abstract
Therapies targeting the RAF-MEK-ERK pathway are generally considered to have limited efficacy in KRAS-mutant cancers. However, specific KRAS mutants exhibit distinct behaviors. Notably, KRASG12R pancreatic ductal adenocarcinoma (PDAC) tumors have shown sensitivity to MEK inhibitors (MEKi) in combination with autophagy inhibitors, but a better understanding of the underlying mechanisms is needed to optimize this treatment strategy. Using a systems-level approach, we uncovered a mechanistic explanation for this phenomenon. Due to distinct biophysical properties, KRASG12R had an impaired ability to activate wild-type HRAS and NRAS (WT-RAS) compared with other KRAS mutants, such as KRASG12D. This reduced activation stemmed from the weaker interaction between KRASG12R and guanine exchange factors (SOS), as well as the tumor suppressor neurofibromin (NF1), crucial in regulating WT-RAS activity. The impaired ability to activate WT-RAS led to weaker holistic MAPK signaling in KRASG12R-driven tumors, which conferred increased sensitivity to MEKi. To substantiate the preclinical findings, the utility of MEKi in combination with the autophagy inhibitor hydroxychloroquine was analyzed in patients with KRASG12R-mutated metastatic PDAC. Five of the eight (62.5%) patients treated in first- or second-line settings had a progression-free survival exceeding 6 months. Three patients had impressive disease control: two had stable disease of 11 and 22.7 months, and one achieved a partial response with an 83% decrease in tumor size that lasted for 8.9 months. Overall, this work highlights how systems-based approaches in precision medicine can uncover mechanistic insights to guide the identification of patients with PDAC most likely to benefit from tailored therapeutic strategies. SIGNIFICANCE: The unique sensitivity of KRASG12R-mutant cancers to MEK inhibitors offers a critical advancement in understanding MAPK signaling and paving the way for precision-targeted therapies in previously untreatable contexts. See related commentary by Tiriac and Engle, p. 1817 See related article by Burge et al., p. 1854 See related article by Burge et al., p. 1868.
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 OpenQuestion graph.
Mutant and Wild-Type RAS Cross-talk and Stoichiometric Deficiencies Are Determinants of Sensitivity to Targeted Therapies in KRASG12R Pancreatic Ductal Adenocarcinoma. · full record | OpenQuestion