Evidence map›Paper›PMID 35195258›Full record

ArticleCancer research2022

Understanding Drug Sensitivity and Tackling Resistance in Cancer.

Jeffrey W Tyner, Franziska Haderk, Anbarasu Kumaraswamy, Linda B Baughn, Brian Van Ness, Song Liu, Himangi Marathe, Joshi J Alumkal, Trever G Bivona, Keith Syson Chan and 5 more

Abstract read
In one paragraph

Article in Cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed.

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  20. Increased Expression ofIranian journal of public health · 2025
    Article
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

15 authors.

Jeffrey W Tyner *Knight Cancer Institute, Oregon Health & Science University, Portland, Oregon.ORCID 0000-0002-2133-0960
Franziska Haderk *Department of Medicine, University of California, San Francisco, San Francisco, California.
Anbarasu Kumaraswamy *Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0002-9997-7430
Linda B Baughn *Division of Hematopathology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Brian Van Ness *Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, Minnesota.
Song Liu *Department of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, New York.
Himangi Marathe *Department of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, New York.
Joshi J AlumkalRogel Cancer Center, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0003-1278-0166
Trever G BivonaDepartment of Medicine, University of California, San Francisco, San Francisco, California.
Keith Syson ChanCedars-Sinai Samuel Oschin Comprehensive Cancer Institute, Los Angeles, California.
Brian J DrukerKnight Cancer Institute, Oregon Health & Science University, Portland, Oregon.ORCID 0000-0001-8331-8206
Alan D HutsonDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0002-7353-5650
Peter S NelsonDivision of Oncology, Department of Medicine, University of Washington, Seattle, Washington.ORCID 0000-0002-5451-5726
Charles L SawyersHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York City, New York.ORCID 0000-0003-4955-6475
Christopher D WilleyDepartment of Radiation Oncology, University of Alabama at Birmingham, Birmingham, Alabama.ORCID 0000-0001-9953-0279

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Understanding the origins of rapid recurrence of pancreatic cancer after resectionP30CA069533 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Luiz Eduardo Bertassoni · 1997 to 2026
$60.5M
Tissue/InformaticsP50CA186786 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Ganesh S Palapattu · 2014 to 2026
$27.6M
Tumor Intrinsic and Microenvironmental Mechanisms Driving Drug Combination Efficacy and Resistance in AMLU54CA224019 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI BRIAN J DRUKER, Shannon K. McWeeney · 2017 to 2026
$13.9M
UCSF Project 1U54CA224081 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Trever G Bivona, Jack Roth · 2017 to 2026
$12.9M
Immuno-Oncology Translation Network: Data Management and Resource-Sharing Center at RPCIU24CA232979 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI HUTSON, ALAN DAVID, LIU, SONG · 2018 to 2024
$8.9M
University of Texas PDX Development and Trial CenterU54CA224065 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DAMODARAN, SENTHILKUMAR, MERIC-BERNSTAM, FUNDA · 2017 to 2022
$7.7M
The MSKCC-UW/Fred Hutch Prostate Cancer Drug Resistance and Sensitivity CenterU54CA224079 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SAWYERS, CHARLES L. · 2017 to 2021
$6.8M
Project 2U54CA224068 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI CORCORAN, RYAN BRUCE, FLAHERTY, KEITH T · 2017 to 2021
$6.3M
Project 3 - Modeling Proteasome Inhibitor Response and Resistance in Cell Lines and Patient Samples with Single Cell Analysis of SubpopulationsU54CA224018 · NCI · MAYO CLINIC ARIZONA · PI KUMAR, SHAJI KUNNATHU · 2017 to 2021
$6.0M
Studying the initiation, progression and therapy of lung cancer in mouse modelsR01CA131261 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI MARTIN MCMAHON · 2009 to 2026
$5.3M
A Rational Systematic Approach to Find Combinations of Pharmacologic and Immune Therapies that Target Identifiable Oncogenic StatesU01CA217885 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI COHEN, EZRA, KAUFMAN, DAN S. · 2017 to 2021
$5.1M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA069533NCI NIH HHS P50 CA186786NCI NIH HHS R01 CA131261NCI NIH HHS R01 CA175397NCI NIH HHS R01 CA192844NCI NIH HHS R01 CA207757NCI NIH HHS R01 CA255609NCI NIH HHS R01 CA262758NCI NIH HHS R37 CA230617NCI NIH HHS U01 CA217885NCI NIH HHS U01 CA223976NCI NIH HHS U01 CA231776NCI NIH HHS U24 CA232979NCI NIH HHS U54 CA224018NCI NIH HHS U54 CA224019NCI NIH HHS U54 CA224065NCI NIH HHS U54 CA224068NCI NIH HHS U54 CA224079NCI NIH HHS U54 CA224081
6 · The paper itself

Abstract

Decades of research into the molecular mechanisms of cancer and the development of novel therapeutics have yielded a number of remarkable successes. However, our ability to broadly assign effective, rationally targeted therapies in a personalized manner remains elusive for many patients, and drug resistance persists as a major problem. This is in part due to the well-documented heterogeneity of cancer, including the diversity of tumor cell lineages and cell states, the spectrum of somatic mutations, the complexity of microenvironments, and immune-suppressive features and immune repertoires, which collectively require numerous different therapeutic approaches. Here, we describe a framework to understand the types and biological causes of resistance, providing translational opportunities to tackle drug resistance by rational therapeutic strategies.

Indexed as

NeoplasmsDrug Resistance, NeoplasmHumansProteomicsTumor Microenvironment

Identifiers

PMID35195258
PMCPMC9018544

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 OpenQuestion graph.