Evidence map›Paper›PMID 41959199›Full record

ArticlebioRxiv : the preprint server for biology2026

c-MYC is an aggregation-prone, amyloidogenic protein.

Ling Lin, Kun-Han Chuang, Chengkai Dai

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

3 authors.

Ling LinMouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA.
Kun-Han ChuangMouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA.
Chengkai DaiMouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA.

Funding

Preservation of Proteomic Stability and Promotion of Protein Lipidation by HSF1ZIABC011767 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DAI, CHENGKAI · 2017 to 2025
$10.3M
Intramural NIH HHS ZIA BC011767
6 · The paper itself

Abstract

The transcription factor c-MYC is a central regulator of diverse biological processes and an oncogenic driver. Paradoxically, c-MYC also exhibits intrinsic tumor-suppressive activity through apoptosis, a phenomenon known as the "c-MYC paradox". Here, we identify c-MYC as an intrinsically amyloidogenic protein. Under proteotoxic stress, c-MYC becomes detergent-insoluble aggregates. Notably, even in the absence of stress, c-MYC assembles into soluble amyloid-like oligomers in human cancer tissues and Alzheimer's disease brains.

Identifiers

PMID41959199
PMCPMC13060799

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.