Evidence map›Paper›PMID 41491203›Full record

ReviewCell communication and signaling : CCS2026

Harnessing nanomedicine to target NF-κB signalling in cancer: at the intersection of inflammatory signalling, metabolic reprogramming, and therapeutic innovation.

Bandari BharathwajChetty, Babu Santha Aswani, Shweta S Shinde, Mohammed S Alqahtani, Mohamed Abbas, Gautam Sethi, Zhaowu Ma, Ajaikumar B Kunnumakkara

Erratum issuedAbstract readReview
In one paragraph

Review in Cell communication and signaling : CCS, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Bandari BharathwajChettyDepartment of Biosciences and Bioengineering, Cancer Biology Laboratory, Indian Institute of Technology Guwahati (IITG), Guwahati, Assam, 781039, India.ORCID http://orcid.org/0000-0002-4147-3993
Babu Santha AswaniDepartment of Biosciences and Bioengineering, Cancer Biology Laboratory, Indian Institute of Technology Guwahati (IITG), Guwahati, Assam, 781039, India.ORCID http://orcid.org/0009-0003-2763-5671
Shweta S ShindeDepartment of Biosciences and Bioengineering, Cancer Biology Laboratory, Indian Institute of Technology Guwahati (IITG), Guwahati, Assam, 781039, India.
Mohammed S AlqahtaniRadiological Sciences Department, College of Applied Medical Sciences, King Khalid University, Abha, 61421, Saudi Arabia.
Mohamed AbbasElectrical Engineering Department, College of Engineering, King Khalid University, Abha, 61421, Saudi Arabia.
Gautam SethiDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, 117600, Singapore.ORCID http://orcid.org/0000-0002-8677-8475
Zhaowu MaSchool of Basic Medicine, Health Science Center, Yangtze University, Jingzhou, 434023, China. mazw@yangtzeu.edu.cn.
Ajaikumar B KunnumakkaraDepartment of Biosciences and Bioengineering, Cancer Biology Laboratory, Indian Institute of Technology Guwahati (IITG), Guwahati, Assam, 781039, India. kunnumakkara@iitg.ac.in.ORCID http://orcid.org/0000-0001-9121-6816

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The nuclear factor kappa B (NF-κB) signalling pathway is a pivotal orchestrator of inflammation, tumour progression, immune modulation, and metabolic reprogramming within the dynamic landscape of the tumour microenvironment (TME). Aberrant and sustained activation of NF-κB is frequently associated with tumour proliferation, resistance to therapy, and poor clinical outcomes. However, conventional NF-κB inhibitors face significant limitations, including systemic toxicity, poor bioavailability, and lack of tumour specificity. Nanomedicine offers a transformative approach to overcome these barriers by enabling the targeted delivery of NF-κB modulators, such as small molecules, RNA interference agents, and gene-editing systems, directly to tumour sites. Recent advances in nanocarriers, including liposomes, polymeric nanoparticles, exosomes, and dendrimers, have demonstrated improved therapeutic indices, enhanced stability, and reduced off-target effects. This review highlights the convergence of nanotechnology, inflammatory signalling, and cancer metabolism, with a focus on how nanomedicine can precisely modulate NF-κB signalling to reprogramme tumour-associated macrophages and remodel the TME. It also discusses preclinical evidence supporting NF-κB-targeted nanomedicine, innovative delivery strategies, and the translational challenges that impede clinical adoption. Collectively, these insights highlight the potential of nanomedicine in advancing NF-κB-targeted cancer therapy by enhancing drug specificity, safety, and therapeutic responsiveness. Future developments integrating artificial intelligence, theranostic design, and personalised nanomedicine are expected to accelerate clinical translation and establish NF-κB-targeted nanotherapeutics as a cornerstone of next-generation precision oncology.Graphical Abstract

Indexed as

InflammationNanomedicineNeoplasmsNF-kappa BSignal TransductionAnimalsHumansMetabolic ReprogrammingTumor MicroenvironmentNF-kappa BImmune reprogrammingNanomedicineNF-κB pathwayTheranosticsTherapeutic resistanceTumour microenvironment

Identifiers

PMID41491203
PMCPMC12870980

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.