Evidence map›Paper›PMID 42380680›Full record

ReviewJournal of cancer research and clinical oncology2026

Nano-biosensors for circulating tumor markers: advancing liquid biopsy toward precision cancer diagnostics.

Taranga Jyoti Baruah, Jutishna Bora, Richa Mishra, SthitiPorna Dutta, Anuj Kumar Borah, Jiwasmika Baishya, ChongthamSovachandra Singh, Indrani Barman, Shailendra Thapliyal, Sumira Malik and 4 more

Abstract readReview
In one paragraph

Review in Journal of cancer research and clinical oncology, 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

14 authors.

Taranga Jyoti Baruah *Department of Microbiology, Royal School of Biosciences, Assam Royal Global University, Guwahati, India.
Jutishna Bora *Amity Institute of Biotechnology, Amity University Jharkhand, Ranchi, India.
Richa MishraDepartment of Computer Engineering, Parul Institute of Engineering and Technology (PIET), Parul University, Waghodia, Vadodara, Gujarat, 391760, India.
SthitiPorna DuttaDepartment of Forensic Science, Royal School of Life Sciences, Assam Royal Global University, Guwahati, India.
Anuj Kumar BorahDepartment of Biotechnology, Royal School of Biosciences, Assam Royal Global University, Guwahati, India.
Jiwasmika BaishyaDepartment of Microbiology, ESIC Medical College and Hospital, Beltola, Guwahati, India.
ChongthamSovachandra SinghDepartment of Biotechnology, Royal School of Biosciences, Assam Royal Global University, Guwahati, India.
Indrani BarmanFaculty of Paramedical Sciences, Assam down town University, Guwahati, India.
Shailendra ThapliyalUttaranchal Institute of Technology, Uttaranchal University, Dehradun, Uttarakhand, 248007, India.
Sumira MalikAmity Institute of Biotechnology, Amity University Jharkhand, Ranchi, India. smalik@rnc.amity.edu.
Subham PreetamDepartment of Chemical Engineering, School of Engineering, Monash University Malaysia, Bandar Sunway, 47500, Selangor, Malaysia.
Dinesh KumarGNA School of Pharmacy, GNA University, Phagwara, Punjab, India. dineshpotlia123@gmail.com.
Neeraj ChoudharyDepartment of Pharmacognosy, GNA School of Pharmacy, GNA University, Phagwara, Punjab, India.
Suresh Babu KondaveetiSymbiosis Medical College for Women & Symbiosis University Hospital and Research Centre, Symbiosis International (Deemed University), Pune, 412115, India. ksuresh.babu@smcw.siu.edu.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early detection of cancer remains a major challenge in oncology. Circulating tumour markers (CTMs), including circulating tumour cells, circulating tumour DNA, exosomes, microRNAs, and tumour-associated proteins, offer a minimally invasive strategy for monitoring tumour dynamics through liquid biopsy. However, their clinical translation is limited by low abundance, heterogeneity, and instability in body fluids. Recent advances in nanotechnology have enabled the development of highly sensitive and specific nano-biosensors that address many of these barriers. This review highlights the current progress in CTM detection using electrochemical, optical, plasmonic, and microfluidic-integrated platforms. Advanced nanomaterials such as graphene, carbon nanotubes, noble metal nanoparticles, quantum dots, and nanozymes are discussed for their roles in signal amplification, surface functionalization, and biomarker selectivity. Special focus is placed on lab-on-a-chip and wearable biosensors for multi-marker, point-of-care testing. To amplify the signals associated with nanobiosensors, various technologies, such as surface functionalization, aptamer and antibody functionalization, and nanozymes, have been integrated with the nanobiosensors.

Indexed as

Biomarkers, TumorBiosensing TechniquesNanotechnologyNeoplasmsPrecision MedicineHumansLiquid BiopsyNanostructuresNeoplastic Cells, CirculatingBiomarkers, TumorBiomarkersBiopsiesCancer detectionCirculating tumour markersNanobiosensors

Identifiers

PMID42380680
PMCPMC13526007

What Socratic holds

Textmetadata
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 Socratic graph.