Evidence map›Paper›PMID 36989217›Full record

ArticlePloS one2023

Functionally distinct BMP1 isoforms show an opposite pattern of abundance in plasma from non-small cell lung cancer subjects and controls.

Margaret K R Donovan, Yingxiang Huang, John E Blume, Jian Wang, Daniel Hornburg, Shadi Ferdosi, Iman Mohtashemi, Sangtae Kim, Marwin Ko, Ryan W Benz and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. 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
5.7field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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  10. The One Hour Human Proteome.Molecular & cellular proteomics : MCP · 2024
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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

15 authors at 1 institution in 1 country.

Margaret K R DonovanSeer, Inc., Redwood City, CA, United States of America.
Yingxiang HuangSeer, Inc., Redwood City, CA, United States of America.
John E BlumeSeer, Inc., Redwood City, CA, United States of America.
Jian WangSeer, Inc., Redwood City, CA, United States of America.
Daniel HornburgSeer, Inc., Redwood City, CA, United States of America.
Shadi FerdosiSeer, Inc., Redwood City, CA, United States of America.ORCID 0000-0003-2933-8809
Iman MohtashemiSeer, Inc., Redwood City, CA, United States of America.
Sangtae KimSeer, Inc., Redwood City, CA, United States of America.
Marwin KoSeer, Inc., Redwood City, CA, United States of America.
Ryan W BenzSeer, Inc., Redwood City, CA, United States of America.
Theodore L PlattSeer, Inc., Redwood City, CA, United States of America.
Serafim BatzoglouSeer, Inc., Redwood City, CA, United States of America.
Luis A DiazThe Ludwig Center and The Howard Hughes Medical Institute at Johns Hopkins Kimmel Cancer Center, Baltimore, MD, United States of America.
Omid C FarokhzadSeer, Inc., Redwood City, CA, United States of America.
Asim SiddiquiSeer, Inc., Redwood City, CA, United States of America.ORCID 0000-0002-0359-2334
Howard Hughes Medical Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advancements in deep plasma proteomics are enabling high-resolution measurement of plasma proteoforms, which may reveal a rich source of novel biomarkers previously concealed by aggregated protein methods. Here, we analyze 188 plasma proteomes from non-small cell lung cancer subjects (NSCLC) and controls to identify NSCLC-associated protein isoforms by examining differentially abundant peptides as a proxy for isoform-specific exon usage. We find four proteins comprised of peptides with opposite patterns of abundance between cancer and control subjects. One of these proteins, BMP1, has known isoforms that can explain this differential pattern, for which the abundance of the NSCLC-associated isoform increases with stage of NSCLC progression. The presence of cancer and control-associated isoforms suggests differential regulation of BMP1 isoforms. The identified BMP1 isoforms have known functional differences, which may reveal insights into mechanisms impacting NSCLC disease progression.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsBiomarkers, TumorBone Morphogenetic Protein 1HumansPeptidesProtein IsoformsBiomarkers, TumorBMP1 protein, humanBone Morphogenetic Protein 1PeptidesProtein Isoforms

Identifiers

PMID36989217
PMCPMC10058078
OpenAlexW4361300671

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.