Evidence map›Paper›PMID 36906600›Full record

ReviewSignal transduction and targeted therapy2023

Tumor cell plasticity in targeted therapy-induced resistance: mechanisms and new strategies.

Zhen-Duo Shi, Kun Pang, Zhuo-Xun Wu, Yang Dong, Lin Hao, Jia-Xin Qin, Wei Wang, Zhe-Sheng Chen, Cong-Hui Han

Open access · goldFull text readReview
In one paragraph

Review in Signal transduction and targeted therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 165 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
165citing papers in PubMed, 2 pooled it
45.5field-weighted citation impact, top 1% of its field
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

165 citing papers in PubMed, 2 syntheses or guidelines pooled it, 201 citations in OpenAlex.

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  6. Malic enzyme 1 senses L-lactate to determine tumor heterogeneity.Signal transduction and targeted therapy · 2026
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  7. Reprogramming resistance in advanced lung cancer: epigenetic modulation to restore therapeutic vulnerability.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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105 more citing papers are in PubMed but not listed here.

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 at 4 institutions in 2 countries.

Zhen-Duo Shi *Department of Urology, Xuzhou Clinical School of Xuzhou Medical University, Jiangsu, China.
Kun Pang *Department of Urology, Xuzhou Clinical School of Xuzhou Medical University, Jiangsu, China.
Zhuo-Xun Wu *Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY, 11439, USA.
Yang Dong *Department of Urology, Xuzhou Clinical School of Xuzhou Medical University, Jiangsu, China.
Lin HaoDepartment of Urology, Xuzhou Clinical School of Xuzhou Medical University, Jiangsu, China.
Jia-Xin QinDepartment of Urology, Xuzhou Clinical School of Xuzhou Medical University, Jiangsu, China.
Wei WangDepartment of Medical College, Southeast University, Nanjing, China.
Zhe-Sheng ChenDepartment of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, NY, 11439, USA. chenz@stjohns.edu.ORCID 0000-0002-8289-097X
Cong-Hui HanDepartment of Urology, Xuzhou Clinical School of Xuzhou Medical University, Jiangsu, China. hanchdoctor@st.btbu.edu.cn.
Xuzhou Medical College · CNJiangsu Normal University · CNSt. John's University · USSoutheast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the success of targeted therapies in cancer treatment, therapy-induced resistance remains a major obstacle to a complete cure. Tumor cells evade treatments and relapse via phenotypic switching driven by intrinsic or induced cell plasticity. Several reversible mechanisms have been proposed to circumvent tumor cell plasticity, including epigenetic modifications, regulation of transcription factors, activation or suppression of key signaling pathways, as well as modification of the tumor environment. Epithelial-to-mesenchymal transition, tumor cell and cancer stem cell formation also serve as roads towards tumor cell plasticity. Corresponding treatment strategies have recently been developed that either target plasticity-related mechanisms or employ combination treatments. In this review, we delineate the formation of tumor cell plasticity and its manipulation of tumor evasion from targeted therapy. We discuss the non-genetic mechanisms of targeted drug-induced tumor cell plasticity in various types of tumors and provide insights into the contribution of tumor cell plasticity to acquired drug resistance. New therapeutic strategies such as inhibition or reversal of tumor cell plasticity are also presented. We also discuss the multitude of clinical trials that are ongoing worldwide with the intention of improving clinical outcomes. These advances provide a direction for developing novel therapeutic strategies and combination therapy regimens that target tumor cell plasticity.

Indexed as

Drug Resistance, NeoplasmNeoplasmsCell PlasticityEpithelial-Mesenchymal TransitionHumansSignal Transduction

Identifiers

PMID36906600
PMCPMC10008648
OpenAlexW4323924126

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read25
identifiers read43
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.