Evidence map›Paper›PMID 41372554›Full record

ReviewCancer gene therapy2026

Pleiotropic effects of all-trans retinoic acid in attenuating the hallmarks of colorectal cancer- challenges and scope of differentiation therapy.

Antony Anista Michael, Pavithra Balakrishnan, Priyadharshini Tamizhmani, Kishore Thirunavukarasu, Selvakumar Subramaniam, Thirunavukkarasu Velusamy

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cancer gene therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Antony Anista MichaelDepartment of Biotechnology, School of Biotechnology and Genetic Engineering, Translational Genomics and Proteomics Laboratory, Bharathiar University, Coimbatore, India.
Pavithra BalakrishnanDepartment of Biotechnology, School of Biotechnology and Genetic Engineering, Translational Genomics and Proteomics Laboratory, Bharathiar University, Coimbatore, India.
Priyadharshini TamizhmaniDepartment of Biotechnology, School of Biotechnology and Genetic Engineering, Translational Genomics and Proteomics Laboratory, Bharathiar University, Coimbatore, India.
Kishore ThirunavukarasuDepartment of Biotechnology, School of Biotechnology and Genetic Engineering, Translational Genomics and Proteomics Laboratory, Bharathiar University, Coimbatore, India.
Selvakumar SubramaniamDepartment of Biochemistry, Molecular Physiology Laboratory, Bharathiar University, Coimbatore, India.
Thirunavukkarasu VelusamyDepartment of Biotechnology, School of Biotechnology and Genetic Engineering, Translational Genomics and Proteomics Laboratory, Bharathiar University, Coimbatore, India. thirunavukkarasu@buc.edu.in.ORCID http://orcid.org/0000-0002-6937-1868

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal Cancer (CRC) is a heterogenous malignancy, attributed by a vast array of mutations that govern the adenoma-carcinoma sequence. The underlying molecular mechanism of CRC recurrence is diverse and complex, in which cancer stem cells (CSCs) remain a major determinant of therapy discontinuation and refractoriness. In contrast to reigning cytotoxic therapies in abolishing cancer cells, leveraging the cytodifferentiation approach offers an effective modality while sparing normal cells. The concept of differentiation therapy fosters from the notion that such cancer stem cells can be either reverted back to their lineage or terminally differentiated cancer cells upon exposure to differentiation inducing agents like All-trans retinoic acid (ATRA). Beyond driving cellular differentiation, ATRA mediates other cellular processes like cell cycle arrest, apoptosis, and abrogates metabolic plasticity, EMT and angiogenesis in cancer cells. These pleiotropic effects of ATRA in modulating the typical hallmarks of cancer and its therapeutic limitations are being studied since 1900s. Despite this, its mode of action and factors impeding its therapeutic effects have not been elucidated in detail and thus remains obscure. However, over the years, various molecular signatures and pathways implicated in the therapeutic effects of ATRA has been unravelled in pieces. In an attempt towards a better picture, the current review aims to highlight the molecular mechanism of ATRA in attenuating the hallmarks of CRC and the factors affecting its therapeutic efficacy from a holistic perspective.

Indexed as

Antineoplastic AgentsCell DifferentiationColorectal NeoplasmsTretinoinAnimalsHumansNeoplastic Stem CellsAntineoplastic AgentsTretinoin

Identifiers

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.