Article · 2024 Paper GEO V2

Proteomics appending a complementary dimension to precision oncotherapy

Computational and Structural Biotechnology Journal

Full Authors

  1. Zhaokai Zhou
  2. Ruiqi Zhang
  3. Aoyang Zhou
  4. Jinxiang Lv
  5. Shuang Chen
  6. Haijiao Zou
  7. Ge Zhang
  8. Ting Lin
  9. Zhan Wang
  10. Yuyuan Zhang
  11. Siyuan Weng
  12. Xinwei Han
  13. Zaoqu Liu

Research Question

How can proteomic measurement and integration with other omics contribute complementary information to precision oncology?

Author Evidence Summary

This narrative review surveys mass spectrometry, aptamer-based assays, proximity extension assays, protein microarrays and combined single-cell methods. It explains how proteomic measurements and computational integration may reveal molecular subtypes, biomarkers, primary-tumor signatures and treatment-related biology. Figures 1-3 and Table 1 organize technologies, analysis and published application examples. The article is a synthesis of earlier research, so application-specific efficacy and accuracy estimates should be traced to their original studies. The review highlights costs, specimen availability and the need for integrated analysis as practical constraints.

Cite this paper

Plain citation

Zhaokai Zhou, Ruiqi Zhang, Aoyang Zhou, Jinxiang Lv, Shuang Chen, Haijiao Zou, Ge Zhang, Ting Lin, Zhan Wang, Yuyuan Zhang, Siyuan Weng, Xinwei Han, Zaoqu Liu. Proteomics appending a complementary dimension to precision oncotherapy. Computational and Structural Biotechnology Journal. 2024. https://doi.org/10.1016/j.csbj.2024.04.044

Author-controlled citation; verify against the publisher version of record.

Evidence Base

Proteomics appending a complementary dimension to precision oncotherapy

Narrative review of proteomic measurement technologies, data integration and potential oncology applications; it reports no new clinical cohort or pooled treatment effect.

technology subsection groups
5
overview figures
3
primary study cohort
Not applicable: narrative review

Counting note

These are review-structure counts, not pooled patient denominators or newly measured performance.

Key Findings

KF1 The review distinguishes major proteomic assay families and their measurement principles.

Secondary technical overview; no head-to-head accuracy comparison is performed.

technology subsection groups
5: mass spectrometry, aptamers, proximity extension assay, protein microarrays, combined single-cell techniques

Source locator: Proteomics analysis technology subsections; Fig. 1A-D

Permalink to KF1

KF2 Proteomic data integration is presented as a way to connect molecular layers and protein-network behavior.

Methodological synthesis of earlier studies rather than a newly trained integrative model.

Evidence for KF2
MeasureValue
illustrated integration methodsTieDIE, PCA and NMF
overview locatorFig. 1E and Fig. 3

Source locator: Proteomics data analysis and integration; Fig. 1E; Future directions for proteomics pairing with other omics; Fig. 3

Permalink to KF2

KF3 The review organizes potential oncology uses including subtyping, primary-site identification, biomarkers and immunotherapy.

Published examples are summarized; clinical utility is not established collectively by this review.

Evidence for KF3
MeasureValue
application-summary tableTable 1
illustrative application figureFig. 2

Source locator: Proteomics in precision oncotherapy subsections; Fig. 2; Table 1; Conclusions

Permalink to KF3

Review Design & Evidence Synthesis

Review profile

Study Design
Narrative technology and application review
Evidence Type
Secondary synthesis of published proteomics studies
Diseases Covered
solid tumors, hematologic malignancies
Translation Scope
Research overview; technology and biomarker hypotheses require application-specific validation

Evidence domains

  • proteomic measurement
  • multi-omics integration
  • molecular classification
  • biomarker discovery
  • cancer immunotherapy

What This Review Adds

  • A technology-to-application map for reading proteomics literature in oncology.
  • A framework for distinguishing assay platforms and secondary evidence from primary clinical validation.

Evidence Scope

Supports

  • An overview of assay principles and integration strategies.
  • Secondary contextualization of published precision-oncology examples.

Does Not Establish

  • A new patient cohort, pooled treatment benefit or meta-analytic accuracy estimate.
  • Clinical superiority of one assay platform for every cancer or use case.
  • Independent validation of all biomarkers discussed in cited primary studies.

Limitations

  • Narrative coverage does not establish a systematic or exhaustive evidence search.
  • No pooled participant denominator or comparative effect estimate is reported.
  • Translation depends on specimen availability, cost and application-specific validation.

When This Study Is Useful to Cite

  1. CU1: Which proteomic approaches does this review cover?

    It covers mass spectrometry, aptamer-based assays, proximity extension assays, protein microarrays and combined single-cell techniques.

    Evidence: KF1

  2. CU2: What role does data integration play in the review?

    Integration connects protein measurements with other molecular layers; the review illustrates approaches including TieDIE, PCA and NMF.

    Evidence: KF2

  3. CU3: Which precision-oncology applications are discussed?

    The review discusses molecular subtyping, primary-site identification, biomarkers, mechanisms and immunotherapy applications using published examples.

    Evidence: KF3

What This Study Should Not Be Cited to Claim

  • A new patient cohort, pooled treatment benefit or meta-analytic accuracy estimate.
  • Clinical superiority of one assay platform for every cancer or use case.
  • Independent validation of all biomarkers discussed in cited primary studies.

Evidence Matrix

Row IDComponentContextFindingEvidence LevelScopeSource LocatorEvidence refs
evidence-kf1The review distinguishes major proteomic assay families and their measurement principles.Secondary technical overview; no head-to-head accuracy comparison is performed.technology subsection groups: 5: mass spectrometry, aptamers, proximity extension assay, protein microarrays, combined single-cell techniquesSecondary synthesis of published proteomics studiesAn overview of assay principles and integration strategies.Proteomics analysis technology subsections; Fig. 1A-DKF1
evidence-kf2Proteomic data integration is presented as a way to connect molecular layers and protein-network behavior.Methodological synthesis of earlier studies rather than a newly trained integrative model.illustrated integration methods: TieDIE, PCA and NMF; overview locator: Fig. 1E and Fig. 3Secondary synthesis of published proteomics studiesSecondary contextualization of published precision-oncology examples.Proteomics data analysis and integration; Fig. 1E; Future directions for proteomics pairing with other omics; Fig. 3KF2
evidence-kf3The review organizes potential oncology uses including subtyping, primary-site identification, biomarkers and immunotherapy.Published examples are summarized; clinical utility is not established collectively by this review.application-summary table: Table 1; illustrative application figure: Fig. 2Secondary synthesis of published proteomics studiesSecondary contextualization of published precision-oncology examples.Proteomics in precision oncotherapy subsections; Fig. 2; Table 1; ConclusionsKF3

Q&A

Which proteomic approaches does this review cover?

It covers mass spectrometry, aptamer-based assays, proximity extension assays, protein microarrays and combined single-cell techniques.

Evidence: KF1

What role does data integration play in the review?

Integration connects protein measurements with other molecular layers; the review illustrates approaches including TieDIE, PCA and NMF.

Evidence: KF2

Which precision-oncology applications are discussed?

The review discusses molecular subtyping, primary-site identification, biomarkers, mechanisms and immunotherapy applications using published examples.

Evidence: KF3

Can this article be cited as a new clinical validation study?

No. It is a narrative synthesis; quantitative claims about individual biomarkers or therapies should be checked against the original primary studies.

Evidence: KF3

Concepts & Entities

Fields

proteomicsprecision oncology

Methods

mass spectrometryproximity extension assayaptamer assaysmulti-omics integration

Related Research

Publication & Provenance

DOI
https://doi.org/10.1016/j.csbj.2024.04.044
Publisher
https://doi.org/10.1016/j.csbj.2024.04.044
PMCID
PMC11058087
Evidence Basis
Formal journal XML and figures/tables text. Original paraphrase only; do not redistribute adapted source figures under CC BY-NC-ND.
Visual Verification Scope
FULL_CORE applies to the selected narrative/structural claims, all supported by article body or text-encoded table. No effect size, cohort size or empirical performance is taken from an image. Visual assets were not inspected; figure references are supplementary locators.
Pmc Url
https://pmc.ncbi.nlm.nih.gov/articles/PMC11058087/
PubMed
https://pubmed.ncbi.nlm.nih.gov/38689716/
Author evidence synthesis of a published narrative review. The reviewed examples are secondary literature; any primary-study effect, validation or treatment claim requires the cited original research.

Study-level evidence table

Study-level author-maintained evidence summary. Not participant-level data and not a ready-to-pool meta-analysis dataset. For formal citation, use the original article DOI.

Download study-level evidence CSV (UTF-8)

Formula safety: cells starting with =, +, -, @ (after leading whitespace), or tab/CR/LF are prefixed with an apostrophe. Treat all cells as text; remove only that safety prefix when recovering the original string.

Verify publication identity

These records identify the same original work; database inclusion is not evidence of scientific validity or clinical benefit.