Evidence map›Paper›PMID 32094544›Full record

ReviewNature reviews. Cancer2020

Tumour heterogeneity and the evolutionary trade-offs of cancer.

Jean Hausser, Uri Alon

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04931446 (Research on Neuroendocrine Neoplasm in a Single Center Based on Multi-omics Integrated Analysis), which is not on this map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed
11.3field-weighted citation impact, top 1% of its field
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.

NCT04931446 unknown statusnot on this mapstarted 2021, after this paper: background citation

Research on Neuroendocrine Neoplasm in a Single Center Based on Multi-omics Integrated Analysis

TypeobservationalSponsorXian-Jun YuRan2021 to 2022Enrolled200ConditionsNeuroendocrine NeoplasmArmsBiopsy/surgical tissue and peripheral blood
3 · Its place in the literature

Who cites it

112 citing papers in PubMed, 221 citations in OpenAlex.

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52 more citing papers are in PubMed but not listed here.

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

2 authors at 2 institutions in 2 countries.

Jean HausserDepartment of Cellular and Molecular Biology, Karolinska Institutet, Solna, Sweden. jean.hausser@ki.se.
Uri AlonDepartment of Molecular and Cell Biology, Weizmann Institute of Science, Rehovot, Israel. uri.alon@weizmann.ac.il.
Karolinska Institutet · SEWeizmann Institute of Science · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumours vary in gene expression programmes and genetic alterations. Understanding this diversity and its biological meaning requires a theoretical framework, which could in turn guide the development of more accurate prognosis and therapy. Here, we review the theory of multi-task evolution of cancer, which is based upon the premise that tumours evolve in the host and face selection trade-offs between multiple biological functions. This theory can help identify the major biological tasks that cancer cells perform and the trade-offs between these tasks. It introduces the concept of specialist tumours, which focus on one task, and generalist tumours, which perform several tasks. Specialist tumours are suggested to be sensitive to therapy targeting their main task. Driver mutations tune gene expression towards specific tasks in a tissue-dependent manner and thus help to determine whether a tumour is specialist or generalist. We discuss potential applications of the theory of multi-task evolution to interpret the spatial organization of tumours and intratumour heterogeneity.

Indexed as

Disease SusceptibilityAnimalsBiomarkers, TumorCell Transformation, NeoplasticGene Expression Regulation, NeoplasticHumansMutationNeoplasmsBiomarkers, Tumor

Identifiers

PMID32094544
OpenAlexW3008217150

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.