Evidence map›Paper›PMID 35361882›Full record

ArticleScientific reports2022

BMP1 is not required for lung fibrosis in mice.

Hsiao-Yen Ma, Elsa-Noah N'Diaye, Patrick Caplazi, Zhiyu Huang, Alexander Arlantico, Surinder Jeet, Aaron Wong, Hans D Brightbill, Qingling Li, Weng Ruth Wong and 5 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Emerging role of BMPs/BMPR2 signaling pathway in treatment for pulmonary fibrosis.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2024
    Review
  4. IGF-II regulates lysyl oxidase propeptide and mediates its effects in part via basic helix-loop-helix E40.Matrix biology : journal of the International Society for Matrix Biology · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Article
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.

Hsiao-Yen Ma *Department of Discovery Immunology, Genentech, South San Francisco, CA, USA.
Elsa-Noah N'Diaye *Department of Discovery Immunology, Genentech, South San Francisco, CA, USA.
Patrick CaplaziDepartment of Pathology, Genentech, South San Francisco, CA, USA.
Zhiyu HuangDepartment of Translational Immunology, Genentech, South San Francisco, CA, USA.
Alexander ArlanticoDepartment of Translational Immunology, Genentech, South San Francisco, CA, USA.
Surinder JeetDepartment of Translational Immunology, Genentech, South San Francisco, CA, USA.
Aaron WongDepartment of Translational Immunology, Genentech, South San Francisco, CA, USA.
Hans D BrightbillDepartment of Translational Immunology, Genentech, South San Francisco, CA, USA.
Qingling LiDepartment of Microchemistry, Proteomics and Lipidomics, Genentech, South San Francisco, CA, USA.
Weng Ruth WongDepartment of Microchemistry, Proteomics and Lipidomics, Genentech, South San Francisco, CA, USA.
Wendy SandovalDepartment of Microchemistry, Proteomics and Lipidomics, Genentech, South San Francisco, CA, USA.
Lucinda TamDepartment of Molecular Biology, Genentech, South San Francisco, CA, USA.
Robert NewmanDepartment of Molecular Biology, Genentech, South San Francisco, CA, USA.
Merone Roose-GirmaDepartment of Molecular Biology, Genentech, South San Francisco, CA, USA.
Ning DingDepartment of Discovery Immunology, Genentech, South San Francisco, CA, USA. ding.ning@gene.com.
Gene Therapy Laboratory · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone morphogenetic protein 1 (BMP1) belongs to the astacin/BMP1/tolloid-like family of zinc metalloproteinases, which play a fundamental role in the development and formation of extracellular matrix (ECM). BMP1 mediates the cleavage of carboxyl terminal (C-term) propeptides from procollagens, a crucial step in fibrillar collagen fiber formation. Blocking BMP1 by small molecule or antibody inhibitors has been linked to anti-fibrotic activity in the preclinical models of skin, kidney and liver fibrosis. Therefore, we reason that BMP1 may be important for the pathogenesis of lung fibrosis and BMP1 could be a potential therapeutic target for progressive fibrotic disease such as idiopathic pulmonary fibrosis (IPF). Here, we observed the increased expression of BMP1 in both human IPF lungs and mouse fibrotic lungs induced by bleomycin. Furthermore, we developed an inducible Bmp1 conditional knockout (cKO) mouse strain. We found that Bmp1 deletion does not protect mice from lung fibrosis triggered by bleomycin. Moreover, we found no significant impact of BMP1 deficiency upon C-term propeptide of type I procollagen (CICP) production in the fibrotic mouse lungs. Based on these results, we propose that BMP1 is not required for lung fibrosis in mice and BMP1 may not be considered a candidate therapeutic target for IPF.

Indexed as

Bone Morphogenetic Protein 1Idiopathic Pulmonary FibrosisAnimalsBleomycinExtracellular MatrixMiceProcollagenBleomycinBmp1 protein, mouseBone Morphogenetic Protein 1Procollagen

Identifiers

PMID35361882
PMCPMC8971496
OpenAlexW4221044690

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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.