Evidence map›Paper›PMID 41593373›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2026

Exploring the therapeutic potential of withaferin A by modulating key oncosignaling pathways.

Prashant Chauhan, Md Nasar Mallick, Safia Obaidur Rab, Mohd Saeed, Fadwa Mohammed Alkhulaifi, Sorabh Lakhanpal, Ajay Singh, Pratibha Pandey, Meenakshi Verma, Fahad Khan

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In one paragraph

Review in Naunyn-Schmiedeberg's archives of pharmacology, 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

10 authors.

Prashant ChauhanMPA Research, 201009, Greater Noida, Uttar Pradesh, India.
Md Nasar MallickDepartment of Pharmacy, School of Medical and Allied Science, Galgotias University, Greater Noida, Uttar Pradesh, 203201, India.
Safia Obaidur RabDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, Abha, Saudi Arabia.
Mohd SaeedDepartment of Biology, College of Science, University of Hail, Hail, Saudi Arabia.
Fadwa Mohammed AlkhulaifiDepartment of Biology, College of Science, Imam Abdulrahman Bin Faisal University, Dammam, P. O. Box 1982, 34212, Saudi Arabia.
Sorabh LakhanpalSchool of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab, India.
Ajay SinghSchool of Applied and Life Sciences, Uttaranchal University, Dehradun, India.
Pratibha PandeyUniversity Centre for Research and Development, Chandigarh University, Gharuan, Mohali, Punjab, 140413, India. shukla.pratibha1985@gmail.com.
Meenakshi VermaUniversity Centre for Research and Development, Chandigarh University, Gharuan, Mohali, Punjab, 140413, India.
Fahad KhanDepartment of Community Medicine, Saveetha Medical College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Tamil Nadu, Chennai, 602105, India. fahadintegralian@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Withaferin A (WA) is an effective withanolide compound derived from Withania somnifera that exhibits a multifaceted pharmacological profile, making it a promising candidate for managing several types of carcinomas. WA has been shown to regulate multiple oncosignaling pathways, proteins, and molecular determinants critical for cancer cell survival, proliferation, and resistance. Its pro-apoptotic, anti-metastasis, antiangiogenic, and anti-proliferative properties demonstrate its efficacy as a multitargeted anticancer agent to manage persistent challenges associated with the complex etiology of cancer. Although several investigations have shown the anticancer efficacy of WA, comprehensive insights into the multitargeted modulation of oncosignaling pathways and synergistic therapeutic potential remain fragmented. Therefore, this review focused on bridging these gaps by providing an integrated overview of WA's mechanistic and translational relevance in cancer therapy. Specifically, this review explores the therapeutic potential of WA in targeting key oncogenic pathways, which are implicated in various types of malignancies. Additionally, this study illustrates the synergistic role of WA in combination with current cancer therapies including immunotherapy, radiation, and chemoradiotherapy. Alongside investigating WA's pharmacological potential as an anticancer agent, this study also examines its pharmacokinetics, bioavailability, and toxicity profile.

Indexed as

Antineoplastic Agents, PhytogenicNeoplasmsWithanolidesAnimalsHumansSignal TransductionAntineoplastic Agents, Phytogenicwithaferin AWithanolidesAnticancerNatural compoundOncosignaling pathwaysPharmacokineticWithaferin A

Identifiers

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.