Evidence map›Paper›PMID 22975008›Full record

ReviewCurrent biology : CB2012

Cellular hyperproliferation and cancer as evolutionary variables.

Alejandro Sánchez Alvarado

Abstract readReview
In one paragraph

Review in Current biology : CB, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. The Elephant and the Spandrel.Evolution, medicine, and public health · 2025
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Cancer progression as a sequence of atavistic reversions.BioEssays : news and reviews in molecular, cellular and developmental biology · 2021
    Article
  7. Evolution, kidney development, and chronic kidney disease.Seminars in cell & developmental biology · 2019
    Review
  8. Article
  9. Article
  10. Evolutionary Nephrology.Kidney international reports · 2017
    Article
  11. Review
  12. Article
  13. Review
  14. Ancient hot and cold genes and chemotherapy resistance emergence.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  15. Article
  16. Evolutionary determinants of cancer.Cancer discovery · 2015
    Review
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

1 author.

Alejandro Sánchez AlvaradoHoward Hughes Medical Institute and Stowers Institute for Medical Research, Kansas City, MO 64110, USA. asa@stowers.org

Funding

The molecular basis of planarian regenerationR37GM057260 · NIGMS · UNIVERSITY OF UTAH · PI SANCHEZ ALVARADO, ALEJANDRO · 2009 to 2018
$2.8M
Howard Hughes Medical InstituteNIGMS NIH HHS R37 GM057260NIGMS NIH HHS R37 GM57260
6 · The paper itself

Abstract

Technological advances in biology have begun to dramatically change the way we think about evolution, development, health and disease. The ability to sequence the genomes of many individuals within a population, and across multiple species, has opened the door to the possibility of answering some long-standing and perplexing questions about our own genetic heritage. One such question revolves around the nature of cellular hyperproliferation. This cellular behavior is used to effect wound healing in most animals, as well as, in some animals, the regeneration of lost body parts. Yet at the same time, cellular hyperproliferation is the fundamental pathological condition responsible for cancers in humans. Here, I will discuss why microevolution, macroevolution and developmental biology all have to be taken into consideration when interpreting studies of both normal and malignant hyperproliferation. I will also illustrate how a synthesis of evolutionary sciences and developmental biology through the study of diverse model organisms can inform our understanding of both health and disease.

Indexed as

Biological EvolutionCell ProliferationAnimalsHelminth ProteinsNeoplasmsPlanariansTumor Suppressor Protein p53Helminth ProteinsTumor Suppressor Protein p53

Identifiers

PMID22975008
PMCPMC3590310

What OpenQuestion holds

Textmetadata
LicenceTDM
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.