Evidence map›Paper›PMID 42611087›Full record

ReviewSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2026

Mechanisms and therapeutic potential of therapy-induced cellular senescence in radiotherapy- and chemotherapy-related alimentary tract mucositis.

Baohan Xie, Zhengqiang Li, Guichao Zhang, Yaping Yin, Lei Chen, Zhaoqiang Zhang

Abstract readReview
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In one paragraph

Review in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Baohan Xie *Department of Oral and Maxillofacial Surgery, Stomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, P. R. China.
Zhengqiang Li *Department of Oral and Maxillofacial Surgery, Stomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, P. R. China.
Guichao ZhangDepartment of Oral and Maxillofacial Surgery, Stomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, P. R. China.
Yaping YinDepartment of Oral and Maxillofacial Surgery, Stomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, P. R. China.
Lei ChenDepartment of Burn, Wound Repair & Reconstruction, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, P. R. China. chenlei8@mail.sysu.edu.cn.
Zhaoqiang ZhangDepartment of Oral and Maxillofacial Surgery, Stomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, P. R. China. 187234415@qq.com.ORCID http://orcid.org/0000-0002-9183-7273

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeRadiotherapy- and chemotherapy-related alimentary tract mucositis is a common complication of cancer treatment, yet the role of cellular senescence during these treatments and post-treatment mucosal repair has not been systematically discussed. This narrative review summarizes the potential involvement of therapy-induced cellular senescence (TIS) in cumulative mucosal injury during treatment and in post-treatment healing and remodeling, and discusses the therapeutic potential and limitations of targeting senescence.

methodsThis narrative review synthesizes evidence from studies on TIS, SASP biology, oral and gastrointestinal mucositis, oxidative stress, extracellular matrix remodeling, microbial dysbiosis, mucosal wound repair, and senescence-targeted interventions.

resultsTIS may amplify mucosal injury during treatment by sustaining ROS accumulation and oxidative stress, contributing to extracellular matrix remodeling, and promoting dysbiosis-prone mucosal microecological remodeling. During post-treatment healing, transient senescence may support immune recruitment, debris clearance, and repair initiation, whereas persistent senescence may maintain inflammatory SASP signaling, impair epithelial regeneration, and promote abnormal tissue remodeling. These processes may operate in both oral and gastrointestinal mucositis, but their dominant cellular sources, microbial interfaces, and repair programs are likely organ-specific. Current experimental evidence also suggests that senescence-targeted strategies may attenuate mucosal injury, although their timing and safety remain critical issues.

conclusionTIS may contribute to both the cumulative injury phase during treatment and the healing and remodeling phase after treatment in alimentary tract mucositis. Senescence-targeted strategies have therapeutic potential, but their translation requires careful consideration of intervention timing, local delivery, tumor safety, and preservation of early repair-promoting senescence.

Indexed as

Antineoplastic AgentsCellular SenescenceGastrointestinal DiseasesMucositisAnimalsHumansNeoplasmsOxidative StressRadiotherapyWound HealingAntineoplastic AgentsGastrointestinal mucositisOral mucositisSenescence-associated secretory phenotypeSenescence-targeted therapyTherapy-induced senescence

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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.