Evidence map›Paper›PMID 40506240›Full record

ArticleJournal of nuclear medicine : official publication, Society of Nuclear Medicine2025

Translational Potential of Fluorescent PARP1 Inhibitor as a Molecular Contrast Agent for Diagnosis of Basal Cell Carcinoma.

Miriam Ricanati, Ucalene Harris, Neil M Neumann, Banu Farabi, Nicholas Kurtansky, Anthony Rossi, Chih-Shan J Chen, Melissa P Pulitzer, Milind Rajadhyaksha, Stephen Dusza and 2 more

Abstract read
In one paragraph

Article in Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 2025. 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.

Miriam RicanatiDermatology Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Ucalene HarrisDermatology Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Neil M NeumannDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Banu FarabiDepartment of Dermatology, New York Medical College, Valhalla, New York; and.
Nicholas KurtanskyDermatology Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Anthony RossiDermatology Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Chih-Shan J ChenDermatology Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Melissa P PulitzerDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Milind RajadhyakshaDermatology Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Stephen DuszaDermatology Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Ashish DhirOffice of Entrepreneurship and Commercialization, Memorial Sloan Kettering Cancer Center, New York, New York jainm@mskcc.org dhira@mskcc.org.
Manu JainDermatology Service, Memorial Sloan Kettering Cancer Center, New York, New York; jainm@mskcc.org dhira@mskcc.org.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Basal cell carcinoma (BCC), the most common skin cancer, typically requires biopsy for definitive diagnosis. Reflectance confocal microscopy is a noninvasive rule-out test, but the lack of nuclear contrast in BCC often leads to missed diagnoses. Our previous research in ex vivo human skin indicated that PARPi-FL, a poly(adenosine diphosphate ribose) polymerase 1 (PARP1) inhibitor-targeted fluorescent contrast agent, penetrated intact skin when applied topically and improved the diagnosis of BCC compared with reflectance confocal microscopy alone. This study refined PARPi-FL's concentration and application timing to assess its detectability, safety, and feasibility for topical use in clinics and investigated its potential to distinguish BCC from nonmalignant clinical mimickers.

Indexed as

Basal Cell CarcinomaContrast MediaFluorescent DyesPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) Polymerase InhibitorsSkin NeoplasmsTranslational Research, BiomedicalAnimalsFemaleHumansMaleMiceMicroscopy, ConfocalContrast MediaFluorescent DyesPARP1 protein, humanPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) Polymerase Inhibitorsbasal cell carcinomabenign lesionsPARPi-FL topical safetySKH1-Hrhr micetranslational potentialYorkshire pigs

Identifiers

PMID40506240
PMCPMC12320582

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.