Evidence map›Paper›PMID 35361803›Full record

ArticleScientific reports2022

Collateral responses to classical cytotoxic chemotherapies are heterogeneous and sensitivities are sparse.

Simona Dalin, Beatrice Grauman-Boss, Douglas A Lauffenburger, Michael T Hemann

Abstract read
In one paragraph

Article in Scientific reports, 2022. 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.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

4 authors.

Simona DalinDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA.
Beatrice Grauman-BossDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA.
Douglas A LauffenburgerDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA. lauffen@mit.edu.
Michael T HemannDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA. hemann@mit.edu.

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Paula T Hammond · 1985 to 2026
$93.9M
Quantitative and functional characterization of therapeutic resistance in cancerU54CA217377 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MANALIS, SCOTT R · 2017 to 2021
$10.2M
Identifying and targeting evolutionary trajectories in cancerR01CA233477 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HEMANN, MICHAEL · 2019 to 2023
$1.7M
NCI NIH HHS NCI U54-CA217377NCI NIH HHS P30 CA014051NCI NIH HHS R01 CA233477NCI NIH HHS U54 CA217377
6 · The paper itself

Abstract

Chemotherapy resistance is a major obstacle to curing cancer patients. Combination drug regimens have shown promise as a method to overcome resistance; however, to date only some cancers have been cured with this method. Collateral sensitivity-the phenomenon whereby resistance to one drug is co-occurrent with sensitivity to a second drug-has been gaining traction as a promising new concept to guide rational design of combination regimens. Here we evolved over 100 subclones of the Eµ-Myc; p19

Indexed as

Antineoplastic AgentsDrug Resistance, NeoplasmCisplatinHumansPaclitaxelVincristineAntineoplastic AgentsCisplatinPaclitaxelVincristine

Identifiers

PMID35361803
PMCPMC8971507

What OpenQuestion holds

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Registered trials

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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.