Evidence map›Paper›PMID 35312779›Full record

ArticleMolecular cancer therapeutics2022

Comprehensive Surfaceome Profiling to Identify and Validate Novel Cell-Surface Targets in Osteosarcoma.

Yifei Wang, Xiangjun Tian, Wendong Zhang, Zhongting Zhang, Rossana Lazcano, Pooja Hingorani, Michael E Roth, Jonathan D Gill, Douglas J Harrison, Zhaohui Xu and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 31 citations in OpenAlex.

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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

25 authors at 6 institutions in 2 countries.

Yifei WangDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Xiangjun TianDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Wendong ZhangDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Zhongting ZhangDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Rossana LazcanoDepartments of Pathology & Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Pooja HingoraniDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-4772-7456
Michael E RothDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-6411-8353
Jonathan D GillDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-7796-8632
Douglas J HarrisonDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Zhaohui XuDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Sylvester JusuDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Sankaranarayanan KannanDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jing WangDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Alexander J LazarDepartments of Pathology & Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-6395-4499
Eric J EarleyRTI International, Research Triangle Park, North Carolina.ORCID 0000-0001-6576-1319
Stephen W EricksonRTI International, Research Triangle Park, North Carolina.ORCID 0000-0001-7602-1770
Tara GelbBicycle Therapeutics, Lexington, Massachusetts.
Philip HuxleyBicycle Therapeutics, Babraham Research Campus, Cambridge, United Kingdom.
Johanna LahdenrantaBicycle Therapeutics, Lexington, Massachusetts.ORCID 0000-0002-2172-5399
Gemma MuddBicycle Therapeutics, Babraham Research Campus, Cambridge, United Kingdom.ORCID 0000-0002-5075-1625
Raushan T KurmashevaGreehey Children's Cancer Research Institute, The University of Texas Health Science Center at San Antonio, San Antonio, Texas.ORCID 0000-0003-3212-2363
Peter J HoughtonGreehey Children's Cancer Research Institute, The University of Texas Health Science Center at San Antonio, San Antonio, Texas.
Malcolm A SmithCancer Therapy Evaluation Program, NCI, Bethesda, Maryland.ORCID 0000-0001-9880-9876
Edward A KolbDivision of Pediatric Hematology/Oncology, A.I. duPont Hospital for Children, Wilmington, Delaware.ORCID 0000-0003-2854-9014
Richard GorlickDepartment of Pediatrics, Children's Cancer Hospital, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-8995-2929
The University of Texas MD Anderson Cancer Center · USBicycle Therapeutics (United Kingdom) · GBRTI International · USThe University of Texas Health Science Center at San Antonio · USCommunity Health Systems - Dupont Hospital · USTracer Technologies (United States) · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Osteosarcoma: Patient Derived Xenograft Preclinical TestingU01CA199221 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Richard G. Gorlick · 2015 to 2026
$3.8M
Orbitrap Elite High-Resolution Mass Spectrometer for Proteomics and MetabolomicsS10OD012304 · OD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HAWKE, DAVID H · 2013 to 2013
$877k
NCI NIH HHS P30 CA016672NCI NIH HHS U01 CA199221NIH HHS S10 OD012304
6 · The paper itself

Abstract

Immunoconjugates targeting cell-surface antigens have demonstrated clinical activity to enable regulatory approval in several solid and hematologic malignancies. We hypothesize that a rigorous and comprehensive surfaceome profiling approach to identify osteosarcoma-specific cell-surface antigens can similarly enable development of effective therapeutics in this disease. Herein, we describe an integrated proteomic and transcriptomic surfaceome profiling approach to identify cell-surface proteins that are highly expressed in osteosarcoma but minimally expressed on normal tissues. Using this approach, we identified targets that are highly expressed in osteosarcoma. Three targets, MT1-MMP, CD276, and MRC2, were validated as overexpressed in osteosarcoma. Furthermore, we tested BT1769, an MT1-MMP-targeted Bicycle toxin conjugate, in osteosarcoma patient-derived xenograft models. The results showed that BT1769 had encouraging antitumor activity, high affinity for its target, and a favorable pharmacokinetic profile. This confirms the hypothesis that our approach identifies novel targets with significant therapeutic potential in osteosarcoma.

Indexed as

Bone NeoplasmsOsteosarcomaAntigens, SurfaceB7 AntigensCell Line, TumorHumansMatrix Metalloproteinase 14ProteomicsAntigens, SurfaceB7 AntigensCD276 protein, humanMatrix Metalloproteinase 14

Identifiers

PMID35312779
PMCPMC9167717
OpenAlexW4220844511

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.