Evidence map›Paper›PMID 41959498›Full record

ArticlebioRxiv : the preprint server for biology2026

Do drugs with biliary toxicity cause cholangiocarcinoma?

Cai Zong, Kyumin Lim, Sierra A Walker, Rui Dai, Mi Ho Jeong, Reanna George, Jung Hyun Jo, Shams Iqbal, Hyungsoon Im, Ralph Weissleder

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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.

Cai ZongCenter for Systems Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Kyumin LimCenter for Systems Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Sierra A WalkerCenter for Systems Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Rui DaiCenter for Systems Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Mi Ho JeongCenter for Systems Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Reanna GeorgeCenter for Systems Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Jung Hyun JoCenter for Systems Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Shams IqbalCenter for Systems Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Hyungsoon ImCenter for Systems Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
Ralph WeisslederCenter for Systems Biology, Massachusetts General Hospital, Boston, MA 02114, USA.

Funding

Training Grant in Molecular Imaging Research (MGH/HMS)T32CA079443 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2000 to 2025
$10.1M
CaNCURE: Cancer Nanomedicine Co-ops For Undergraduate Research ExperiencesR25CA174650 · NCI · NORTHEASTERN UNIVERSITY · PI SRINIVAS SRIDHAR · 2014 to 2026
$3.4M
Development of plasmon-enhanced biosensing for multiplexed profiling of extracellular vesiclesR01GM138778 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI IM, HYUNGSOON · 2020 to 2024
$2.3M
Pancreatic cancer patient-derived xenograft tumors for translational studies in precision cancer medicineR01CA293063 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Andrew Liss, RALPH WEISSLEDER, MD, PhD · 2025 to 2026
$1.3M
Nano-CRISPR extracellular vesicle sensing system for longitudinal tumor monitoringR33CA281794 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Hyungsoon Im · 2024 to 2026
$1.2M
Bioorthogonal probe development for highly parallel in vivo imagingR33CA277820 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2023 to 2025
$1.2M
NCI NIH HHS R01 CA293063NCI NIH HHS R25 CA174650NCI NIH HHS R33 CA277820NCI NIH HHS R33 CA281794NCI NIH HHS T32 CA079443NIGMS NIH HHS R01 GM138778
6 · The paper itself

Abstract

Many commonly used therapeutic drugs cause biliary toxicity, but it is unclear if they are directly responsible for the increasing incidence of cholangiocarcinoma (CCA). We tested experimentally and analyzed through a cohort approach whether drugs, such as the commonly used antibiotic Augmentin, which is a poster-child of biliary toxicity, are causally linked to CCA development. Using sophisticated analytical tools in cholangiocytes, including single extracellular vesicle (EV) analysis, we found no evidence that Augmentin increases the cholangiocyte malignancy marker YAP1 or phospho-YAP1. Furthermore, we analyzed the CCA incidence in our healthcare system and determined it to be 0.0932% (Augmentin group) and 0.0799% (amoxicillin control group). Although the Augmentin group showed a numerically higher CCA incidence, the association did not reach statistical significance (RR = 1.1669, 95% CI 0.6200-2.1961; Fisher's exact test, P = 0.7493). Similarly, we found no evidence for cholangiocarcinoma development with other commonly used drugs, including chlorpromazine, floxuridine, 5-fluorouracil, flucloxacillin and terbinafine. We conclude that there is no direct causal relationship between clinical Augmentin doses and CCA development.

Indexed as

antibioticcancercholangiocarcinomadrug toxicity

Identifiers

PMID41959498
PMCPMC13060385

What OpenQuestion holds

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LicenceCC BY
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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.