Evidence map›Paper›PMID 42073629›Full record

ArticleCancers2026

Development of a Telehealth-Enabled Portable Optical Endomicroscopy System with Targeted Peptides: A Preclinical Feasibility Study for Cervical Cancer Detection.

Chanchai Thaijiam, Nitipon Navaitthiporn, Preeyarat Rithcharung, Nicholas Piyawattanametha, Shoji Komai, Supang Khondee, Wibool Piyawattanametha

Abstract read
In one paragraph

Article in Cancers, 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

7 authors.

Chanchai ThaijiamFaculty of Engineering, Srinakharinwirot University, Ongkharak Campus, Nakorn Nayok 26120, Thailand.
Nitipon NavaitthipornAdvanced Imaging Research Center, School of Engineering, King Mongkut's Institute of Technology Ladkrabang, Ladkrabang, Bangkok 10520, Thailand.
Preeyarat RithcharungAdvanced Imaging Research Center, School of Engineering, King Mongkut's Institute of Technology Ladkrabang, Ladkrabang, Bangkok 10520, Thailand.
Nicholas PiyawattanamethaSchool of Engineering, Michigan State University, East Lansing, MI 48824, USA.
Shoji KomaiDepartment of Information Technology, Faculty of Technology, International Professional University of Technology, Tokyo 1-7-3 Nishi-Shinjuku, Shinjuku 160-0023, Tokyo, Japan.
Supang KhondeeSchool of Pharmaceutical Sciences, University of Phayao, Maeka, Phayao 56000, Thailand.
Wibool PiyawattanamethaAdvanced Imaging Research Center, School of Engineering, King Mongkut's Institute of Technology Ladkrabang, Ladkrabang, Bangkok 10520, Thailand.ORCID 0000-0002-2228-8485

Funding

Japan Science and Technology Agency JPMJPR09G7KMITL Research and Innovation Services 64226National Research Council of Thailand 38700Program Management Unit for Competitiveness 175749Technology and Innovation-Based Enterprise Development Fund 183091
6 · The paper itself

Abstract

BACKGROUND/

objectivesWe developed a telehealth-enabled fiber-bundle endomicroscopy platform and evaluated its preclinical feasibility for targeted fluorescence imaging in cervical cancer models.

methodsThe platform integrates a portable fiber-bundle endomicroscopy (FBE) system, fluorescein isothiocyanate (FITC)-labeled candidate peptides, and a secure web-based telehealth platform for remote consultation. The FBE probe achieved a field of view of 1,700 µm and a lateral resolution of 4 µm, enabling cellular-level fluorescence imaging in a compact, portable format. Four FITC-labeled peptides (SHS1*, SHS2*, FPP*, and CRL*) were evaluated in A549, SiHa, and CaSki cell lines. Ex vivo testing was performed on commercial cervical tissue-array samples. The telehealth platform was assessed for secure medical-image/video transmission and end-to-end latency in a simulated remote-consultation setting.

resultsAmong the tested probes, FPP*-FITC and CRL*-FITC showed higher fluorescence-positive fractions in the p16-overexpressing cervical cancer cell lines than in the A549 comparator line, with the strongest signals observed in CaSki cells. In ex vivo testing, CRL*-FITC generated higher fluorescence intensity in malignant cervical tissue-array samples than in non-malignant comparator tissues, with a reported 4.6- to 7.4-fold difference in mean signal intensity (

conclusionsThese results support the technical and preclinical feasibility of integrating targeted fluorescence imaging, portable fiber-bundle endomicroscopy, and telehealth into a single platform. This study should therefore be interpreted as a preclinical feasibility study evaluating optical, molecular, and telehealth integration, rather than as a clinically validated cervical cancer screening test.

Indexed as

cervical cancerfluorescence imagingoptical endomicroscopytargeted peptidetelehealth

Identifiers

PMID42073629
PMCPMC13115089

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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.