Evidence map›Paper›PMID 41591758›Full record

ArticleClinical and translational science2026

Pacific Blue Derivatives of Paclitaxel as Fluorescent Probes of OATP1B-Type Transporters.

Mahesh R Nepal, Yue Xu, Yan Jin, Peng Hu, Xiaojun Hu, Digamber S Rane, Angelo E Andres, Eman A Ahmed, Brandon Steiger, Alex Sparreboom and 2 more

Abstract read
In one paragraph

Article in Clinical and translational science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Mahesh R NepalDivision of Pharmaceutics and Pharmacology, The Ohio State University, Columbus, Ohio, USA.
Yue XuDivision of Pharmaceutics and Pharmacology, The Ohio State University, Columbus, Ohio, USA.ORCID 0000-0003-2755-4719
Yan JinDivision of Pharmaceutics and Pharmacology, The Ohio State University, Columbus, Ohio, USA.
Peng HuDivision of Pharmaceutics and Pharmacology, The Ohio State University, Columbus, Ohio, USA.
Xiaojun HuDivision of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, Ohio, USA.
Digamber S RaneDivision of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, Ohio, USA.
Angelo E AndresDivision of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, Ohio, USA.
Eman A AhmedDivision of Pharmaceutics and Pharmacology, The Ohio State University, Columbus, Ohio, USA.
Brandon SteigerDivision of Pharmaceutics and Pharmacology, The Ohio State University, Columbus, Ohio, USA.
Alex SparreboomDivision of Pharmaceutics and Pharmacology, The Ohio State University, Columbus, Ohio, USA.ORCID 0000-0003-2660-6644
Blake R PetersonDivision of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, Ohio, USA.
Shuiying HuDivision of Pharmaceutics and Pharmacology, The Ohio State University, Columbus, Ohio, USA.ORCID 0000-0002-9806-7734

Funding

Targeting neuronal transport to ameliorate vincristine neurotoxicityR01CA272254 · NCI · OHIO STATE UNIVERSITY · PI Sharyn D Baker, Shuiying Hu · 2023 to 2026
$2.6M
NCI NIH HHS R01 CA272254
6 · The paper itself

Abstract

Paclitaxel (Taxol) is a widely used anticancer agent that undergoes extensive hepatic metabolism and that causes a debilitating, dose-limiting peripheral neurotoxicity. We previously reported that the uptake of paclitaxel in hepatocytes and dorsal root ganglion neurons, the site of injury within the nervous system, is mediated by the organic anion transporting polypeptides OATP1B1 and OATP1B3 (Oatp1b2 in rodents), transporters that are highly sensitive to pharmacological inhibition. To facilitate future screens of chemical libraries to identify modulators and imaging-based drug distribution studies, we explored the utility of PB-Gly-Taxol and PB-GABA-Taxol, derivatives of paclitaxel linked to the coumarin-derived fluorophore Pacific Blue, as in vitro and in vivo substitute biomarker probes of paclitaxel. Transport studies in transfected HEK293 cells revealed efficient uptake of these PB-taxoids by human and murine OATP1B/Oatp1b-type transporters, with up to 100-fold increases in uptake relative to values observed in vector control cells, and inhibition of this transport by known inhibitors. Although cell viability assays demonstrated lower cytotoxicity of both PB-taxoids (IC

Indexed as

Fluorescent DyesLiver-Specific Organic Anion Transporter 1PaclitaxelSolute Carrier Organic Anion Transporter Family Member 1B3AnimalsBiological TransportFluorescent Chemosensor CompoundsHEK293 CellsHumansMiceOrganic Cation Transport ProteinsFluorescent Chemosensor CompoundsFluorescent DyesLiver-Specific Organic Anion Transporter 1Organic Cation Transport ProteinsPaclitaxelSLCO1A1 protein, mouseSLCO1B1 protein, humanSlco1b2 protein, mouseSLCO1B3 protein, humanSolute Carrier Organic Anion Transporter Family Member 1B3drug transportersOATP1BPacific bluepaclitaxel

Identifiers

PMID41591758
PMCPMC12840550

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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 OpenQuestion graph.