Evidence map›Paper›PMID 42261393›Full record

ArticleFrontiers in toxicology2026

Evaluation and investigation of the cardiotoxicity of the potential anti-cholangiocarcinoma drug lanatoside C.

Yu-Hai Ma, Chong-Fei Huang, Hai-Dong Ma, Jin-Yu Zhao, Wen-An Wang, Zi-He Dong, Yi Shao, Long Gao, Jian-Jun Chen, Wen-Bo Meng

Abstract read
In one paragraph

Article in Frontiers in toxicology, 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.

Yu-Hai MaThe First Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Chong-Fei HuangThe First Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Hai-Dong MaThe First Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Jin-Yu ZhaoThe First Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Wen-An WangThe First Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Zi-He DongThe First Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Yi ShaoThe First Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Long GaoThe First Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.
Jian-Jun ChenState Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, China.
Wen-Bo MengThe First Clinical Medical College, Lanzhou University, Lanzhou, Gansu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Lanatoside C (Lan C), a cardiac glycoside, has demonstrated potent anti-cholangiocarcinoma activity. However, its potential cardiotoxicity at therapeutic doses remains poorly understood. This study aimed to systematically evaluate the cardiotoxicity of Lan C at cellular and organ levels and to elucidate its underlying molecular mechanisms. Methods: Human AC16 cardiomyocytes (ATCC® CRL-3568™) were employed for Results: Lan C showed a dose-dependent inhibitory effect Conclusion: Lan C exhibits measurable but relatively low cardiotoxicity at concentrations effective against cholangiocarcinoma, with cardiac effects may be manageable at therapeutic doses. These findings support Lan C as a promising anti-tumor candidate with controllable cardiotoxicity under optimized dosing and clinical monitoring.

Indexed as

apoptosiscardiotoxicitycholangiocarcinomalanatoside Cmitochondrial membrane potential

Identifiers

PMID42261393
PMCPMC13242897

What OpenQuestion holds

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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.