Evidence map›Paper›PMID 41060425›Full record

ReviewCancer metastasis reviews2025

Spatial proteomics for investigating solid tumor resistance mechanisms.

Xin Ming M Zhou, Anjali J D'Amiano, Charles Lu, Vrinda Madan, Sara Khoshniyati, Jack Kollings, Noah E Sunshine, Sachin S Surwase, Joel C Sunshine

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cancer metastasis reviews, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

9 authors.

Xin Ming M ZhouDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.ORCID 0009-0003-1020-068X
Anjali J D'AmianoDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.ORCID 0009-0007-9692-9306
Charles LuDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.ORCID 0000-0003-3450-1682
Vrinda MadanDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.ORCID 0000-0002-7962-1752
Sara KhoshniyatiDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.ORCID 0009-0007-0148-2055
Jack KollingsDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.ORCID 0009-0008-6598-377X
Noah E SunshineDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA.
Sachin S SurwaseTranslational ImmunoEngineering Center, Johns Hopkins University School of Medicine, Baltimore, MD, 21231, USA.ORCID 0000-0003-2129-3992
Joel C SunshineDepartment of Dermatology, Johns Hopkins University School of Medicine, Baltimore, MD, 21287, USA. joelsunshine@jhmi.edu.ORCID 0000-0001-9987-6712

Funding

A PLATFORM TECHNOLOGY TO GENETICALLY REPROGRAM CANCER CELLS FOR ENHANCED IMMUNOTHERAPYR37CA246699 · NCI · JOHNS HOPKINS UNIVERSITY · PI TZENG, STEPHANY YI · 2020 to 2025
$2.6M
NIH HHS R37CA246699
6 · The paper itself

Abstract

Spatial proteomics technologies have been pivotal in profiling tumor immune microenvironments at single-cell resolution, advancing our understanding of cancer biology, identifying key cell populations in solid tumors, and predicting treatment responses. Although immune checkpoint and molecular inhibitors have revolutionized cancer care, resistance mechanisms remain a major therapeutic challenge that hinder productive responses in a notable fraction of cancer patients. In this review, we outline current spatial proteomics and computational analysis tools for studying the tumor immune microenvironment and discuss how spatial proteomics techniques have helped elucidate cancer resistance mechanisms across multiple tumor types. In this process, we highlight the importance of investigating immunosuppressive cell populations that can mediate cancer resistance, specifically with regard to their localization, protein signatures, and surrounding interactions. Finally, we provide a look ahead at future applications of artificial intelligence/machine learning and multi-omics approaches that will help further propel our understanding of cancer resistance mechanisms through spatial biology research.

Indexed as

Drug Resistance, NeoplasmNeoplasmsProteomicsAnimalsHumansTumor MicroenvironmentCancer resistanceImmunotherapyProteomicsSpatial biology

Identifiers

What OpenQuestion holds

Textmetadata
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.