Evidence map›Paper›PMID 39243400›Full record

ArticleInternational journal of cancer2025

Enhanced pharmacological activities of AKR1C3-activated prodrug AST-3424 in cancer cells with defective DNA repair.

Fanying Meng, Tianyang Qi, Xing Liu, Yizhi Wang, Jibing Yu, Zhaoqiang Lu, Xiaohong Cai, Anrong Li, Don Jung, Jianxin Duan

Abstract read
In one paragraph

Article in International journal of cancer, 2025. 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. Article
  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.

Fanying MengAscentawits Pharmaceuticals, LTD, Shenzhen, China.ORCID 0009-0005-1849-1834
Tianyang QiAscentawits Pharmaceuticals, LTD, Shenzhen, China.
Xing LiuAscentawits Pharmaceuticals, LTD, Shenzhen, China.
Yizhi WangAscentawits Pharmaceuticals, LTD, Shenzhen, China.
Jibing YuAscentawits Pharmaceuticals, LTD, Shenzhen, China.
Zhaoqiang LuAscentawits Pharmaceuticals, LTD, Shenzhen, China.
Xiaohong CaiAscentawits Pharmaceuticals, LTD, Shenzhen, China.
Anrong LiAscentawits Pharmaceuticals, LTD, Shenzhen, China.
Don JungAscentawits Pharmaceuticals, LTD, Shenzhen, China.
Jianxin DuanAscentawits Pharmaceuticals, LTD, Shenzhen, China.

Funding

Development and Reform Commission of Shenzhen Municipality XMHT20220104029Development and Reform Commission of Shenzhen Municipality XMHT20220104047
6 · The paper itself

Abstract

AST-3424 is a novel and highly tumor-selective prodrug. AST-3424 is activated by AKR1C3 to release a toxic bis-alkylating moiety, AST 2660. In this study, we have investigated the essential role of DNA repair in AST-3424 mediated pharmacological activities in vitro and in vivo. We show here that AST-3424 is effective as a single therapeutic agent against cancer cells to induce cytotoxicity, DNA damage, apoptosis and cell cycle arrest at G2 phase in a dose- and AKR1C3-dependent manner in both p53-proficient H460 (RRID:CVCL_0459) and p53-deficient HT-29 cells (RRID:CVCL_0320). The combination of abrogators of G2 checkpoint with AST-3424 was only synergistic in HT-29 but not in H460 cells. The enhanced activity of AST-3424 in HT-29 cells was due to impaired DNA repair ability via the attenuation of cell cycle G2 arrest and reduced RAD51 expression. Furthermore, we utilized a BRCA2 deficient cell line and two PDX models with BRCA deleterious mutations to study the increased activity of AST-3424. The results showed that AST-3424 exhibited enhanced in vitro cytotoxicity and superior and durable in vivo anti-tumor effects in cells deficient of DNA repair protein BRCA2. In summary, we report here that when DNA repair capacity is reduced, the in vitro and in vivo activity of AST-3424 can be further enhanced, thus providing supporting evidence for the further evaluation of AST-3424 in the clinic.

Indexed as

Aldo-Keto Reductase Family 1 Member C3ApoptosisDNA RepairProdrugsXenograft Model Antitumor AssaysAnimalsAntineoplastic AgentsCell Line, TumorDNA DamageG2 Phase Cell Cycle CheckpointsHT29 CellsHumansMiceNeoplasmsAKR1C3 protein, humanAldo-Keto Reductase Family 1 Member C3Antineoplastic AgentsProdrugsAKR1C3AST‐3424cell cyclesDNA repairp53

Identifiers

PMID39243400
PMCPMC11578084

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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.