Evidence map›Paper›PMID 41772145›Full record

ArticleActa pharmacologica Sinica2026

Chloroethylnitrosourea analogue HJ03 overcomes temozolomide resistance of glioblastoma in mice through induction of ferroptosis and apoptosis.

Heng Yang, Yi Cao, Wei Zhao, Ying-Fan Wen, Yan Wu, Ting Wang, Li-Zhi Zhu, Yong-Dong Zou, Bao-Min Xi, Duo Zheng

Abstract read
In one paragraph

Article in Acta pharmacologica Sinica, 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
–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

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

10 authors.

Heng Yang *Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Base for International Science and Technology Cooperation: Carson Cancer Stem Cell Vaccines R&D Center, International Cancer Center, Shenzhen Key Laboratory of Translational Medicine in Oncology, School of Basic Medical Sciences, School of Pharmaceutical Sciences, Medical School; College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, 518035, China.
Yi Cao *Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Base for International Science and Technology Cooperation: Carson Cancer Stem Cell Vaccines R&D Center, International Cancer Center, Shenzhen Key Laboratory of Translational Medicine in Oncology, School of Basic Medical Sciences, School of Pharmaceutical Sciences, Medical School; College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, 518035, China.
Wei Zhao *Guangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Base for International Science and Technology Cooperation: Carson Cancer Stem Cell Vaccines R&D Center, International Cancer Center, Shenzhen Key Laboratory of Translational Medicine in Oncology, School of Basic Medical Sciences, School of Pharmaceutical Sciences, Medical School; College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, 518035, China.
Ying-Fan WenGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Base for International Science and Technology Cooperation: Carson Cancer Stem Cell Vaccines R&D Center, International Cancer Center, Shenzhen Key Laboratory of Translational Medicine in Oncology, School of Basic Medical Sciences, School of Pharmaceutical Sciences, Medical School; College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, 518035, China.
Yan WuGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Base for International Science and Technology Cooperation: Carson Cancer Stem Cell Vaccines R&D Center, International Cancer Center, Shenzhen Key Laboratory of Translational Medicine in Oncology, School of Basic Medical Sciences, School of Pharmaceutical Sciences, Medical School; College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, 518035, China.
Ting WangGuangzhou KemRocMed Co., Ltd., Guangzhou, 510320, China.
Li-Zhi ZhuGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Base for International Science and Technology Cooperation: Carson Cancer Stem Cell Vaccines R&D Center, International Cancer Center, Shenzhen Key Laboratory of Translational Medicine in Oncology, School of Basic Medical Sciences, School of Pharmaceutical Sciences, Medical School; College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, 518035, China. lzzhu86@pku.edu.cn.
Yong-Dong ZouGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Base for International Science and Technology Cooperation: Carson Cancer Stem Cell Vaccines R&D Center, International Cancer Center, Shenzhen Key Laboratory of Translational Medicine in Oncology, School of Basic Medical Sciences, School of Pharmaceutical Sciences, Medical School; College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, 518035, China. zouyd@szu.edu.cn.
Bao-Min XiGuangdong Provincial Key Laboratory of New Drug Screening, Guangzhou Key Laboratory of Drug Research for Emerging Virus Prevention and Treatment, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, 510515, China. xibaomin@smu.edu.cn.
Duo ZhengGuangdong Provincial Key Laboratory of Genome Stability and Disease Prevention, Base for International Science and Technology Cooperation: Carson Cancer Stem Cell Vaccines R&D Center, International Cancer Center, Shenzhen Key Laboratory of Translational Medicine in Oncology, School of Basic Medical Sciences, School of Pharmaceutical Sciences, Medical School; College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, 518035, China. dzheng@szu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Surgery followed by adjuvant chemoradiation is the standard treatment for glioblastoma multiforme (GBM). Temozolomide (TMZ) is the only first-line chemotherapeutic drug approved by the US Food and Drug Administration for the treatment of GBM. Acquired chemoresistance to TMZ is the primary cause of treatment failure, resulting in recurrence and a poor prognosis. O6-methylguanine DNA methyltransferase (MGMT) overexpression and loss of function mutations targeting mismatch repair (MMR) are the major mechanisms TMZ-resistance found in GBM cells. In this study we developed a new alkylating agent that could overcome TMZ resistance. We designed a new chloroethylnitrosourea analog HJ03, and demonstrated that HJ03 was more potent than TMZ in inhibiting GBM cell lines U251 (MGMT

Indexed as

Antineoplastic Agents, AlkylatingApoptosisBrain NeoplasmsDrug Resistance, NeoplasmFerroptosisGlioblastomaNitrosourea CompoundsTemozolomideAnimalsCell Line, TumorHumansMiceMice, NudeAntineoplastic Agents, AlkylatingNitrosourea CompoundsTemozolomidechloroethylnitrosourea analog HJ03DNA damageferroptosisgliomaMGMTtemozolomide resistance

Identifiers

PMID41772145
PMCPMC13279786

What Socratic holds

Textmetadata
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 Socratic graph.