Evidence map›Paper›PMID 41655222›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

OCIAD2 Stabilizes Integrin β1 Signaling Through SNX17-Mediated Endosomal Recycling to Lipid Rafts and Modulates Cisplatin Response in HNSCC.

Li Cui, Shanshan Si, Min Ye, Pei Lin, Meiyan Zou, Yunfan Lin, Xu Chen, Bing Guo, Wenjuan Sun, Xinyuan Zhao

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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

10 authors.

Li CuiStomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, Guangdong, China.
Shanshan SiStomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, Guangdong, China.
Min YeStomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, Guangdong, China.
Pei LinStomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, Guangdong, China.
Meiyan ZouStomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, Guangdong, China.
Yunfan LinStomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, Guangdong, China.
Xu ChenStomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, Guangdong, China.
Bing GuoDepartment of Dentistry, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Wenjuan SunDepartment of Stomatology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xinyuan ZhaoStomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0003-4770-8877

Funding

Guangdong Provincial Science and Technology Project Foundation 2022A0505050038National Natural Science Foundation of China 82372905National Natural Science Foundation of China 82573074Science and Technology Program of Guangzhou 2025A04J3464Young Top-notch Talent of Pearl River Talent Plan 0920220228
6 · The paper itself

Abstract

While cisplatin is a widely used and effective chemotherapeutic agent in the treatment of head and neck squamous cell carcinoma (HNSCC), the molecular mechanisms underlying its resistance remain poorly understood. In this study, we identify OCIA domain containing 2 (OCIAD2) as a central mediator of chemoresistance and tumor progression in HNSCC. Through transcriptomic analysis and Co-immunoprecipitation coupled with mass spectrometry, we demonstrate that OCIAD2 modulates integrin signaling by directly interacting with integrin β1. Mechanistic investigations reveal that OCIAD2 does not regulate integrin β1 at the transcriptional level, but instead stabilizes its protein expression by preventing lysosomal degradation and enhancing its recycling. Importantly, OCIAD2 binds to SNX17 and enhances its association with integrin β1, promoting its recycling to lipid raft-enriched regions of the plasma membrane. By maintaining integrin β1 in these lipid raft compartments, OCIAD2 sustains the activation of the FAK-PI3K-AKT-mTOR signaling cascade, thereby fostering cellular resilience and resistance to cisplatin. Moreover, targeting OCIAD2, either through genetic silencing or RNA-based therapies, significantly sensitizes tumors to cisplatin treatment in preclinical models. This study uncovers a previously unrecognized trafficking-dependent mechanism of drug resistance, suggesting that OCIAD2 may serve as a novel therapeutic target to overcome chemoresistance in HNSCC.

Indexed as

CisplatinHead and Neck NeoplasmsIntegrin beta1Membrane MicrodomainsSorting NexinsSquamous Cell Carcinoma of Head and NeckAnimalsAntineoplastic AgentsCell Line, TumorDrug Resistance, NeoplasmEndosomesHumansMiceSignal TransductionAntineoplastic AgentsCisplatinIntegrin beta1Sorting Nexinscisplatin responseHNSCCintegrin β1OCIA domain containing 2SNX17

Identifiers

PMID41655222
PMCPMC13067770

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.