Evidence map›Paper›PMID 41514380›Full record

ArticleBiomarker research2026

Machine learning-driven proteomics classifier deciphers tumor origins of primary and metastatic squamous cell carcinomas.

Tianqi Gong, I Weng Lao, Chan Fong Chio, Xiaowei Zhang, Min Ren, Weiwei Li, Ning Qu, Xiaotian Ni, Tongqing Gong, Yanzi Gu and 17 more

Abstract read
In one paragraph

Article in Biomarker research, 2026. 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

27 authors.

Tianqi Gong *Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
I Weng Lao *Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Chan Fong Chio *Department of Anatomical Pathology, Conde de São Januário Hospital, Macau, SAR, 999078, China.
Xiaowei Zhang *Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Min Ren *Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Weiwei Li *Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Ning Qu *Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Xiaotian NiNational Center for Protein Sciences Beijing, Beijing, 102206, PR China.
Tongqing GongNational Center for Protein Sciences Beijing, Beijing, 102206, PR China.
Yanzi GuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Guangqi QinDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Xiaoqun YangDepartment of Pathology, School of Medicine, Ruijin Hospital, Shanghai JiaoTong University, Shanghai, 200025, China.
Yu DengDepartment of Pathology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310003, China.
Yan XuDepartment of Pathology, Shanghai Oriental Hospital, Tongji University, Shanghai, 200032, China.
Zebing LiuDepartment of Pathology, Renji Hospital, School of Medicine, Shanghai JiaoTong University, Shanghai, 200127, China.
Kun TaoDepartment of Pathology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, 200032, China.
Yingyong HouDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Sio In WongDepartment of Anatomical Pathology, Conde de São Januário Hospital, Macau, SAR, 999078, China.
Qifeng WangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Wenfeng WangCancer Institute, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Jian WangDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Yuan LiDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Wenxing QinDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China. qinwenxingqwx@163.com.
Zhiguo LuoDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China. luozhiguo88@163.com.
Xiaoyan ZhouDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. xyzhou100@163.com.
Jun QinInstitutes of Biomedical Sciences, Fudan university, Shanghai, 200032, China. jqin1965@126.com.
Midie XuDepartment of Pathology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. xumd27202003@sina.com.

Funding

Beijing Xisike Clinical Oncology Research Foundation Young2023-0023Innovation Program of STCSM Shanghai Science and Technology Committee 20Z11900300National Natural Science Foundation of China 82272626National Natural Science Foundation of China 82573699Shanghai Clinical Research Project of Shanghai Shenkang Hospital Development Center SHDC2020CR4068
6 · The paper itself

Abstract

Squamous cell carcinoma (SCC) occurs across multiple organs with highly similar histology, making the diagnosis of SCC of unknown primary (SCCUP) particularly challenging. To address this, we established a machine learning–based 39-protein biomarker classifier (39PBC) trained on proteomic profiles from 387 SCC samples collected at seven tertiary hospitals. The classifier accurately predicted the origin of primary and metastatic SCCs from cervical, esophageal, lung, nasopharyngeal, and head and neck sites, with validation in internal (n = 324) and external (n = 63) cohorts yielding AUCs of 0.924–0.961 and 0.971 and accuracies above 87%. Immunohistochemistry of 509 cases further identified a simplified five-marker panel (four robust site-specific markers CCDC6, LGALS7, LGALS9, and P16, together with EBER) suitable for routine screening. Importantly, 39PBC demonstrated reliable performance in real-world SCCUP and dual-primary cases. Proteomic profiling also uncovered distinct prognostic and molecular landscapes, implicating metabolic activation as a driver of progression and immune modulation as a site-specific feature. Together, these findings establish a clinically applicable workflow that integrates high-resolution proteomics with practical IHC validation, offering a public resource to improve SCCUP diagnosis, enable cost-effective clinical translation, and provide mechanistic insights into SCC metastasis.

Indexed as

ClassifierMachine learningMetastasisProteomicsSquamous cell carcinomaTumor origin

Identifiers

PMID41514380
PMCPMC12809902

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.