Evidence map›Paper›PMID 42055323›Full record

ArticleThe Journal of biological chemistry2026

Platelet CLEC-2 activation leads to GPIb⍺ shedding: Implications for doxorubicin chemotherapy and thrombosis.

Zackary Rousseau, Wenjing Ma, Tianle Long, Sladjana Slavkovic, Xin Qiu, Xiaomei Lao, Xun Grace Wu, Kaishiv Joshi, Yunqing Amelia Zhu, Guangheng Zhu and 2 more

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 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

12 authors.

Zackary RousseauDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; Department of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada; Toronto Platelet Immunobiology Group, Toronto, Ontario, Canada.
Wenjing MaDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; Department of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada; Toronto Platelet Immunobiology Group, Toronto, Ontario, Canada. Electronic address: Wj_m@outlook.com.
Tianle LongDepartment of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada; Toronto Platelet Immunobiology Group, Toronto, Ontario, Canada.
Sladjana SlavkovicDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; Department of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada; Toronto Platelet Immunobiology Group, Toronto, Ontario, Canada; Canadian Blood Services Centre for Innovation, Toronto, Ontario, Canada.
Xin QiuDepartment of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada; Toronto Platelet Immunobiology Group, Toronto, Ontario, Canada.
Xiaomei LaoDepartment of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada; Toronto Platelet Immunobiology Group, Toronto, Ontario, Canada.
Xun Grace WuDepartment of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada; Toronto Platelet Immunobiology Group, Toronto, Ontario, Canada.
Kaishiv JoshiDepartment of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada; Toronto Platelet Immunobiology Group, Toronto, Ontario, Canada.
Yunqing Amelia ZhuDepartment of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada; Toronto Platelet Immunobiology Group, Toronto, Ontario, Canada.
Guangheng ZhuDepartment of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada; Toronto Platelet Immunobiology Group, Toronto, Ontario, Canada.
Kelsie L ThuDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; Department of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada.
Heyu NiDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada; Department of Laboratory Medicine, LKSKI-Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada; Toronto Platelet Immunobiology Group, Toronto, Ontario, Canada; Canadian Blood Services Centre for Innovation, Toronto, Ontario, Canada; Department of Physiology, University of Toronto, Toronto, Ontario, Canada; Department of Medicine, University of Toronto, Toronto, Ontario, Canada. Electronic address: Heyu.Ni@unityhealth.to.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Doxorubicin (Dox) is a potent first-line chemotherapeutic and widely administered against different types of cancer, but is associated with a myriad of side effects, including cancer/chemotherapy-associated thrombosis and drug-induced thrombocytopenia. Although we and others have reported Dox-induced platelet activation, the binding partner of Dox on platelets has not been previously explored. Here, we found human and mouse platelet aggregation triggered via C-type lectin-like receptor-2 (CLEC-2) was obstructed by Dox, but aggregation induced by classical agonists like ADP, collagen/collagen-related peptide, or thrombin receptor-activating peptide 6, was unaffected. By isothermal titration calorimetry, we detected a high binding affinity between Dox and recombinant CLEC-2 at 4.2 ± 2.4 nM. Interestingly, we found significant GPIb⍺ shedding from human and mouse platelet surfaces following Dox treatment. Consistently, GPIb⍺ shedding was recapitulated following anti-CLEC-2 monoclonal antibody treatment. Using Piceatannol to selectively inhibit CLEC-2 intracellular signaling or the pan-matrix metalloproteinases inhibitor GM6001 rescued glycoprotein Ibα (GPIbα) from both Dox and CLEC-2 mAb-induced shedding. Using GI254023X or GW280264X to specifically inhibit ADAM10 or ADAMs10/17, respectively, revealed inhibition of ADAM10/17, but not ADAM10 exclusively, prohibited GPIbα shedding. Collectively, this implicates the classical sheddase of GPIbα, ADAM17. Thus, we pinpointed CLEC-2 as a binding partner for Dox on platelets and a novel pathway of ADAM17-mediated GPIb⍺ shedding via CLEC-2. These data not only provide insights into a mechanism of Dox-induced platelet activation, thrombosis, and drug-induced thrombocytopenia, but also reveal putative precision therapeutic approaches for Dox-treated patients and nominate CLEC-2 inhibition as a means to regulate thrombotic disease and/or bleeding disorders.

Indexed as

Antibiotics, AntineoplasticBlood PlateletsDoxorubicinLectins, C-TypePlatelet Glycoprotein GPIb-IX ComplexThrombosisAnimalsHumansMembrane GlycoproteinsMiceMice, Inbred C57BLPlatelet ActivationPlatelet AggregationAntibiotics, AntineoplasticCLEC2B protein, humanCLEC-2 protein, mouseDoxorubicinLectins, C-TypeMembrane GlycoproteinsPlatelet Glycoprotein GPIb-IX ComplexADAM17CLEC-2doxorubicinGPIbα sheddingintegrin αIIbβ3plateletsthrombocytopeniathrombosis

Identifiers

PMID42055323
PMCPMC13223932

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.