Evidence map›Paper›PMID 40295625›Full record

ArticleScientific reports2025

Isoalantolactone induces the apoptosis of oxaliplatin-resistant human colorectal cancer cells mediated by ROS generation and activation of JNK and p38 MAPK.

Seung-On Lee, Sang Hoon Joo, Na Yeong Lee, Seung-Sik Cho, Goo Yoon, Ki-Taek Kim, Yung Hyun Choi, Jin Woo Park, Joon-Seok Choi, Jung-Hyun Shim

Abstract read
In one paragraph

Article in Scientific reports, 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. Article
  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.

Seung-On Lee *Department of Biomedicine, Health & Life Convergence Sciences, BK21 Four, College of Pharmacy, Mokpo National University, Muan, 58554, Republic of Korea.
Sang Hoon Joo *Department of Pharmacy, College of Pharmacy, Daegu Catholic University, Gyeongsan, 38430, Republic of Korea.
Na Yeong LeeDepartment of Biomedicine, Health & Life Convergence Sciences, BK21 Four, College of Pharmacy, Mokpo National University, Muan, 58554, Republic of Korea.
Seung-Sik ChoDepartment of Biomedicine, Health & Life Convergence Sciences, BK21 Four, College of Pharmacy, Mokpo National University, Muan, 58554, Republic of Korea.
Goo YoonDepartment of Pharmacy, College of Pharmacy, Mokpo National University, Muan, 58554, Republic of Korea.
Ki-Taek KimDepartment of Biomedicine, Health & Life Convergence Sciences, BK21 Four, College of Pharmacy, Mokpo National University, Muan, 58554, Republic of Korea.
Yung Hyun ChoiDepartment of Biochemistry, College of Korean Medicine, Dong-Eui University, Busan, 47227, Republic of Korea.
Jin Woo ParkDepartment of Biomedicine, Health & Life Convergence Sciences, BK21 Four, College of Pharmacy, Mokpo National University, Muan, 58554, Republic of Korea.
Joon-Seok ChoiDepartment of Pharmacy, College of Pharmacy, Daegu Catholic University, Gyeongsan, 38430, Republic of Korea. joonschoi@cu.ac.kr.
Jung-Hyun ShimDepartment of Biomedicine, Health & Life Convergence Sciences, BK21 Four, College of Pharmacy, Mokpo National University, Muan, 58554, Republic of Korea. s1004jh@gmail.com.

Funding

National Research Foundation of Korea RS-2024-00336900
6 · The paper itself

Abstract

Treating colorectal cancer (CRC) poses challenges due to the lack of specific molecular targets. Although oxaliplatin (Ox) is commonly used to treat CRC, resistance frequently develops, necessitating the discovery of new therapeutics. This study explored the anticancer effects of Isoalantolactone (IAL) on human CRC cells HCT116 and Ox-resistant HCT116 (HCT116-OxR). Apoptosis, ROS generation, cell cycle distribution, mitochondrial membrane potential (MMP), and caspase activation were assessed through flow cytometry. Protein levels were determined by Western blot analysis. IAL reduced cell viability, measured by MTT assay, and inhibited anchorage-independent colony formation in CRC cells in a time- and concentration-dependent manner. The IC

Indexed as

Antineoplastic AgentsApoptosisColorectal NeoplasmsDrug Resistance, NeoplasmJNK Mitogen-Activated Protein Kinasesp38 Mitogen-Activated Protein KinasesReactive Oxygen SpeciesCaspasesCell ProliferationCell SurvivalEnzyme ActivationHCT116 CellsHumansMembrane Potential, MitochondrialOxaliplatinSesquiterpenesAntineoplastic AgentsCaspasesisoalantolactoneJNK Mitogen-Activated Protein KinasesOxaliplatinp38 Mitogen-Activated Protein KinasesReactive Oxygen SpeciesSesquiterpenesApoptosisColorectal cancerIsoalantolactoneJNK/p38 MAPKOxaliplatinReactive oxygen species

Identifiers

PMID40295625
PMCPMC12038024

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.