Evidence map›Paper›PMID 35121907›Full record

ArticleNature cancer2021

The Cancer Surfaceome Atlas integrates genomic, functional and drug response data to identify actionable targets.

Zhongyi Hu, Jiao Yuan, Meixiao Long, Junjie Jiang, Youyou Zhang, Tianli Zhang, Mu Xu, Yi Fan, Janos L Tanyi, Kathleen T Montone and 5 more

Open access · greenAbstract read
In one paragraph

Article in Nature cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% 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

79 citing papers in PubMed, 1 synthesis or guideline pooled it, 149 citations in OpenAlex.

  1. Mapping the clinical landscape of multifunctional CAR T cells: Targets, trends, and synergies.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Pooled it
  2. Antibody-drug conjugate engineering: from design to efficacy and safety.Signal transduction and targeted therapy · 2026
    Review
  3. Article
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  10. Identifying a cancer therapeutic target: Cell-SELEX identifies a membrane protein for aptamer-mediated growth suppression.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  17. Review
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19 more citing papers are in PubMed but not listed here.

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 5 institutions in 1 country.

Zhongyi Hu *Center for Research on Reproduction & Women's Health, University of Pennsylvania, Philadelphia, PA, USA.
Jiao Yuan *Center for Research on Reproduction & Women's Health, University of Pennsylvania, Philadelphia, PA, USA.
Meixiao LongDivision of Hematology, Department of Internal Medicine, Ohio State University, Columbus, OH, USA.
Junjie JiangCenter for Research on Reproduction & Women's Health, University of Pennsylvania, Philadelphia, PA, USA.
Youyou ZhangCenter for Research on Reproduction & Women's Health, University of Pennsylvania, Philadelphia, PA, USA.
Tianli ZhangCenter for Research on Reproduction & Women's Health, University of Pennsylvania, Philadelphia, PA, USA.
Mu XuCenter for Research on Reproduction & Women's Health, University of Pennsylvania, Philadelphia, PA, USA.
Yi FanDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0002-6290-0595
Janos L TanyiDepartment of Obstetrics and Gynecology, University of Pennsylvania, Philadelphia, PA, USA.
Kathleen T MontoneDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Omid TavanaBioscience, Research and Early Development, Oncology R&D, AstraZeneca, Waltham, MA, USA.
Ho Man ChanBioscience, Research and Early Development, Oncology R&D, AstraZeneca, Waltham, MA, USA.
Xiaowen HuCenter for Research on Reproduction & Women's Health, University of Pennsylvania, Philadelphia, PA, USA. xiaowenh@upenn.edu.ORCID http://orcid.org/0000-0002-3269-4356
Robert H VonderheideAbramson Cancer Center, University of Pennsylvania, Philadelphia, PA, USA. rhv@upenn.edu.ORCID http://orcid.org/0000-0002-7252-954X
Lin ZhangCenter for Research on Reproduction & Women's Health, University of Pennsylvania, Philadelphia, PA, USA. linzhang@upenn.edu.ORCID http://orcid.org/0000-0003-1998-0611
University of Pennsylvania · USBioscience Research · USCenter for Human Reproduction · USThe Ohio State University · USUPMC Hillman Cancer Center · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Therapeutic Micro RNA Strategies for Ovarian CancerP50CA083638 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI GODWIN, ANDREW K., GOLEMIS, ERICA A. · 1999 to 2013
$33.6M
Radiation and checkpoint blockade for cancer immune therapyP01CA210944 · NCI · UNIVERSITY OF PENNSYLVANIA · PI VONDERHEIDE, ROBERT H · 2017 to 2022
$11.5M
Targeted Combination Therapy for MelanomaP50CA174523 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 2014 to 2018
$11.1M
Molecular Determinants and Therapeutic Consequences of Immune Heterogeneity in CancerR01CA229803 · NCI · UNIVERSITY OF PENNSYLVANIA · PI STANGER, BEN Z · 2018 to 2022
$3.7M
Targeting CDK7 in high-grade serous ovarian carcinomaR01CA262070 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ZHANG, LIN · 2021 to 2025
$2.2M
Molecular mechanism and preclinical development of BETi and PARPi combination therapyR01CA225929 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ZHANG, LIN · 2019 to 2023
$1.8M
The epigenetic mechanism of long non-coding RNA in cancerR01CA190415 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ZHANG, LIN · 2015 to 2019
$1.8M
The role of microRNA, mir-30d, in the initiation and progression of cancerR01CA142776 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ZHANG, LIN · 2010 to 2014
$1.6M
NCI NIH HHS P01 CA210944NCI NIH HHS P30 CA016520NCI NIH HHS P50 CA083638NCI NIH HHS P50 CA174523NCI NIH HHS R01 CA142776NCI NIH HHS R01 CA190415NCI NIH HHS R01 CA225929NCI NIH HHS R01 CA229803NCI NIH HHS R01 CA262070
6 · The paper itself

Abstract

Cell-surface proteins (SPs) are a rich source of immune and targeted therapies. By systematically integrating single-cell and bulk genomics, functional studies and target actionability, in the present study we comprehensively identify and annotate genes encoding SPs (GESPs) pan-cancer. We characterize GESP expression patterns, recurrent genomic alterations, essentiality, receptor-ligand interactions and therapeutic potential. We also find that mRNA expression of GESPs is cancer-type specific and positively correlates with protein expression, and that certain GESP subgroups function as common or specific essential genes for tumor cell growth. We also predict receptor-ligand interactions substantially deregulated in cancer and, using systems biology approaches, we identify cancer-specific GESPs with therapeutic potential. We have made this resource available through the Cancer Surfaceome Atlas ( http://fcgportal.org/TCSA ) within the Functional Cancer Genome data portal.

Indexed as

GenomicsNeoplasmsGenomeHumansLigandsProteomicsLigands

Identifiers

PMID35121907
PMCPMC9940627
OpenAlexW4200116291

What OpenQuestion holds

Textmetadata
LicenceTDM
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.