Evidence map›Paper›PMID 35353015›Full record

ArticleMolecular biology of the cell2022

Cell Painting predicts impact of lung cancer variants.

Juan C Caicedo, John Arevalo, Federica Piccioni, Mark-Anthony Bray, Cathy L Hartland, Xiaoyun Wu, Angela N Brooks, Alice H Berger, Jesse S Boehm, Anne E Carpenter and 1 more

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
19.8field-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.

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

44 citing papers in PubMed, 70 citations in OpenAlex.

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  10. Alternate dyes for image-based profiling assays.SLAS discovery : advancing life sciences R & D · 2025
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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

11 authors at 1 institution in 1 country.

Juan C CaicedoBroad Institute of Harvard and MIT, Cambridge, MA 02142.
John ArevaloBroad Institute of Harvard and MIT, Cambridge, MA 02142.
Federica PiccioniBroad Institute of Harvard and MIT, Cambridge, MA 02142.
Mark-Anthony BrayBroad Institute of Harvard and MIT, Cambridge, MA 02142.
Cathy L HartlandBroad Institute of Harvard and MIT, Cambridge, MA 02142.
Xiaoyun WuBroad Institute of Harvard and MIT, Cambridge, MA 02142.
Angela N BrooksBroad Institute of Harvard and MIT, Cambridge, MA 02142.
Alice H BergerBroad Institute of Harvard and MIT, Cambridge, MA 02142.
Jesse S BoehmBroad Institute of Harvard and MIT, Cambridge, MA 02142.
Anne E CarpenterBroad Institute of Harvard and MIT, Cambridge, MA 02142.
Shantanu SinghBroad Institute of Harvard and MIT, Cambridge, MA 02142.
Broad Institute · US

Funding

Extracting rich information from biological imagesR35GM122547 · NIGMS · BROAD INSTITUTE, INC. · PI Anne E. Carpenter · 2017 to 2026
$6.2M
NIGMS NIH HHS R35 GM122547
6 · The paper itself

Abstract

Most variants in most genes across most organisms have an unknown impact on the function of the corresponding gene. This gap in knowledge is especially acute in cancer, where clinical sequencing of tumors now routinely reveals patient-specific variants whose functional impact on the corresponding genes is unknown, impeding clinical utility. Transcriptional profiling was able to systematically distinguish these variants of unknown significance as impactful vs. neutral in an approach called expression-based variant-impact phenotyping. We profiled a set of lung adenocarcinoma-associated somatic variants using Cell Painting, a morphological profiling assay that captures features of cells based on microscopy using six stains of cell and organelle components. Using deep-learning-extracted features from each cell's image, we found that cell morphological profiling (cmVIP) can predict variants' functional impact and, particularly at the single-cell level, reveals biological insights into variants that can be explored at our public online portal. Given its low cost, convenient implementation, and single-cell resolution, cmVIP profiling therefore seems promising as an avenue for using non-gene specific assays to systematically assess the impact of variants, including disease-associated alleles, on gene function.

Indexed as

Adenocarcinoma of LungLung NeoplasmsAllelesHumansMicroscopyPhenotype

Identifiers

PMID35353015
PMCPMC9265158
OpenAlexW4221003443

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.