Evidence map›Paper›PMID 42538377›Full record

ReviewCell death and differentiation2026

Associative memory plays a role in ER-1α positive breast cancers.

Dan Lu, David Hoyos, Ning Yao, Benjamin Greenbaum, Yael Aylon, Moshe Oren, Arnold J Levine

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cell death and differentiation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Dan Lu *Department of Systems Biology, Blavatnik Institute at Harvard Medical School, Boston, MA, 02115, USA.
David Hoyos *Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Ning YaoMemorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Benjamin GreenbaumMemorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.ORCID http://orcid.org/0000-0001-6153-8793
Yael AylonThe Weizmann Institute, Rehovot, Israel.ORCID http://orcid.org/0000-0001-5821-9548
Moshe OrenThe Weizmann Institute, Rehovot, Israel.ORCID http://orcid.org/0000-0003-4311-7172
Arnold J LevineSimons Center for Systems Biology, Institute for Advanced Study, Princeton, NJ, 08540, USA. alevine@ias.edu.ORCID http://orcid.org/0000-0002-1871-6387

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This perspective brings together multiple observations concerning the regulatory architecture and functional interactions of the TP53 gene and its isoforms. The TP53 gene encompasses an internal enhancer-promoter region (P2) located between exons 2 and 5, which is transactivated by full-length TAp53α, to drive the expression of truncated TP53 isoforms ΔN133p53α, β or γ. ΔN133p53α homo-monomers or dimers very likely form hetero-tetramers with homo-dimers of full-length TAp53α. The TAp53α-ΔN133p53 tetramer then acts as a transcription factor augmenting mitochondrial efficiency, DNA repair, telomere restoration and reversing cellular senescence, thus opposing many outputs of tumor suppressive TAp53α homo-tetramers. Other transcription factors, such as estrogen receptor (ER), OCT1, and SOX9 also may bind the P2 promoter-enhancer to promote transcription of oncogenic TP53 isoforms. These transcription factors, together with full-length TAp53α, appear to cooperate to maintain an open chromatin state in the P2 region in a manner reminiscent of a neural "associative memory" network.

Identifiers

What OpenQuestion holds

Textmetadata
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.