Evidence map›Paper›PMID 42273395›Full record

ArticleBiosensors & bioelectronics: X2025

Hydrogel-based multiplexed high-risk human papillomavirus DNA/RNA detection for cervical cancer screening.

Morteza Azizi, Jae-Sang Hong, Joshua Spitzberg, Ralph Weissleder, Cesar M Castro, Hyungsoon Im

Abstract read
In one paragraph

Article in Biosensors & bioelectronics: X, 2025. 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

6 authors.

Morteza AziziCenter for Systems Biology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Jae-Sang HongCenter for Systems Biology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Joshua SpitzbergCenter for Systems Biology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Ralph WeisslederCenter for Systems Biology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Cesar M CastroCenter for Systems Biology, Massachusetts General Hospital, Boston, MA, 02114, USA.
Hyungsoon ImCenter for Systems Biology, Massachusetts General Hospital, Boston, MA, 02114, USA.ORCID 0000-0002-0626-1346

Funding

Training Grant in Molecular Imaging Research (MGH/HMS)T32CA079443 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2000 to 2025
$10.1M
Technology CoreU54EB034654 · NIBIB · CORNELL UNIVERSITY · PI Saurabh Mehta · 2023 to 2026
$7.0M
Smartphone for molecular cancer diagnostic in AfricaUH3CA202637 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI CHABNER, BRUCE ALLAN, WEISSLEDER, MD, PHD, RALPH · 2018 to 2020
$2.9M
Development of plasmon-enhanced biosensing for multiplexed profiling of extracellular vesiclesR01GM138778 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI IM, HYUNGSOON · 2020 to 2024
$2.3M
Nano-CRISPR extracellular vesicle sensing system for longitudinal tumor monitoringR33CA281794 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI Hyungsoon Im · 2024 to 2026
$1.2M
Nano-plasmonic technology for high-throughput single exosome analysesR21CA217662 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI IM, HYUNGSOON · 2019 to 2021
$585k
NCI NIH HHS R21 CA217662NCI NIH HHS R33 CA281794NCI NIH HHS T32 CA079443NCI NIH HHS UH3 CA202637NIBIB NIH HHS U54 EB034654NIGMS NIH HHS R01 GM138778
6 · The paper itself

Abstract

Rapid triaging of high-risk human papillomavirus (HPV) infections, especially in resource-limited regions, can reduce cervical cancer deaths by identifying high-risk patients and minimizing pathology bottlenecks and overtreatment. Here, we developed a simple, rapid method for parallel detection of HPV DNA and RNA subtypes associated with a high risk of developing cervical cancer. Specifically, we applied loop-mediated isothermal nucleic acid amplification (LAMP) in a hydrogel-based platform (LAMPGel) for HPV DNA or RNA detection using distinct hydrogel chambers within a single chip. The LAMPGel platform locally restricts single HPV gDNA or mRNA strands with a LAMP cocktail, which is then distributed within a thin hydrogel to locally form single fluorescent spots after a short isothermal incubation of <30 min. Detecting and counting these spots identifies HPV infection, viral load, and, more importantly, RNA expression as a predictive marker for cervical cancer development. LAMPGel is a sensitive, specific, easy-to-use, and rapid method for a point-of-care (POC) platform for potential applications in low- and middle-income countries once the technology is further validated with clinical samples in those settings. Furthermore, it could find broader applications in POC nucleic acid assays.

Indexed as

Cervical cancerHPVHydrogelLAMPPoint-of-care detection

Identifiers

PMID42273395
PMCPMC13249390

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.