Evidence map›Paper›PMID 42876954›Full record

ReviewFrontiers in molecular biosciences2026

Gut microbiota-cancer crosstalk: emerging molecular targets for personalized cancer treatment- a comprehensive review.

Pooja Negi, Arpita Upreti, Preeti Budhlakoti, Amit Kumar Sen, Mitali Danu, Sumit Tewari, Nirmal Joshi, Deepak Chandra Joshi

Abstract readReview
In one paragraph

Review in Frontiers in molecular biosciences, 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

8 authors.

Pooja NegiCollege of Pharmacy, Graphic Era Hill University, Bhimtal Campus, Bhimtal, Uttarakhand, India.
Arpita UpretiFaculty of Pharmaceutical Science, Amrapali University, Haldwani, India.
Preeti BudhlakotiVasudev College of Pharmacy, Haldwani, India.
Amit Kumar SenDepartment of Pharmaceutical Chemistry, Samrat Prithviraj Chauhan College of Pharmacy, Kashipur, India.
Mitali DanuFaculty of Pharmaceutical Science, Amrapali University, Haldwani, India.
Sumit TewariVasudev College of Pharmacy, Haldwani, India.
Nirmal JoshiFaculty of Pharmaceutical Science, Amrapali University, Haldwani, India.
Deepak Chandra JoshiDepartment of Pharmacology, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer remains a major global health challenge, and growing evidence indicates that the gut microbiota plays an important role in cancer initiation, progression, metastasis, and response to treatment through complex interactions with host signaling, metabolism, and immunity. This comprehensive narrative review discusses the molecular mechanisms underlying gut microbiota-cancer crosstalk, with particular emphasis on dysbiosis, microbial metabolites, immune modulation, and microbiota-regulated oncogenic pathways, including TLR/NF-κB, Wnt/β-catenin, JAK/STAT, PI3K/Akt/mTOR, and Hippo-YAP signaling. The review also examines emerging molecular targets, including microbial extracellular vesicles, bacterial small RNAs, ferroptosis-related mechanisms, and microbiota-mitochondria interactions. In addition, current microbiota-targeted therapeutic strategies, such as fecal microbiota transplantation, engineered bacterial therapeutics, CRISPR-based microbiome engineering, and microbiome-informed approaches to precision oncology are discussed. Relevant peer-reviewed literature published primarily within the recent 5-year period was considered from major scientific databases and publisher platforms, including PubMed, Scopus, Web of Science, Springer, Elsevier, and MDPI. Overall, the available evidence suggests that gut microbiota represents an important component of the tumor ecosystem and may provide promising biomarkers and therapeutic targets. Integration of microbiome research with multi-omics and artificial intelligence may further support the development of personalized cancer treatment.

Indexed as

artificial intelligencebiomarkerscancergut microbiotamicrobial metabolitespersonalized medicineprecision oncologytumor microenvironment

Identifiers

PMID42876954
PMCPMC13662544

What OpenQuestion 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 OpenQuestion graph.