Evidence map›Paper›PMID 41102953›Full record

ReviewCurrent pharmaceutical design2026

Targeting Key Molecular Mechanisms in Triple-Negative Breast Cancer Therapies with Natural Compounds.

Md Faysal, Mehrukh Zehravi, Md Al Amin, Sherouk Hussein Sweilam, Uttam Prasad Panigrahy, Abdul Sayeed Khan, Nihar Ranjan Kar, Santosh Kumar Dash, Ashutosh Padhan, Safia Obaidur Rab and 3 more

Abstract readReview
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In one paragraph

Review in Current pharmaceutical design, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
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

13 authors.

Md FaysalDepartment of Pharmacy, Faculty of Health and Life Sciences, Daffodil International University, Dhaka, 1207, Bangladesh.
Mehrukh ZehraviDepartment of Clinical Pharmacy, College of Dentistry & Pharmacy, Buraydah Private Colleges, Buraydah, 51418, Saudi Arabia.
Md Al AminDepartment of Pharmacy, Faculty of Health and Life Sciences, Daffodil International University, Dhaka, 1207, Bangladesh.
Sherouk Hussein SweilamDepartment of Pharmacognosy, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al-Kharj, 11942, Saudi Arabia.
Uttam Prasad PanigrahyFaculty of Pharmaceutical Science, Assam Down Town University, Sankar Madhab Path, Gandhi Nagar, Panikhaiti, Guwahati, Assam, India.
Abdul Sayeed KhanDepartment of Pharmaceutics, The Pharmaceutical College, Barpali, Odisha, India.
Nihar Ranjan KarCenturion University of Technology and Management, Gopalpur, Balasore, Odisha, India.
Santosh Kumar DashDepartment of Pharmaceutics, The Pharmaceutical College, Barpali, Odisha, India.
Ashutosh PadhanDepartment of Pharmaceutics, The Pharmaceutical College, Barpali, Odisha, India.
Safia Obaidur RabDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, Abha, Saudi Arabia.
Md Zia UddinDepartment of Pharmacy, Faculty of Pharmaceutical Sciences, University of Science and Technology Chittagong, Chattogram, Bangladesh.
Nezar CherradaDepartment of Molecular and Cellular Biology, Faculty of Life and Natural Sciences, University of El Oued, El-oued, 39000, Algeria.
Talha Bin EmranDepartment of Pharmacy, Faculty of Health and Life Sciences, Daffodil International University, Dhaka, 1207, Bangladesh.

Funding

King Khalid University, Abha, Saudi Arabia R.G.P. 2/480/46
6 · The paper itself

Abstract

backgroundTriple-negative breast cancer (TNBC) is characterized by the absence of HER2 expression, progesterone receptor (PR), and estrogen receptor (ER). TNBC has a poor prognosis and limited therapy options due to its lack of specific targets and aggressive behavior.

aimThis review demonstrates the therapeutic efficacy and mechanisms of natural compounds in targeting key molecular pathways involved in the development and progression of TNBC, investigating their interaction with oncogenic signaling pathways.

methodsA thorough literature review was conducted using databases such as PubMed, Scopus, and Web of Science to identify studies assessing the anti-TNBC properties of natural compounds.

resultsNatural bioactive compounds like curcumin, resveratrol, quercetin, EGCG, berberine, and thymoquinone have demonstrated promising anticancer properties in TNBC models. These limit metastasis, induce apoptosis, inhibit proliferation, and reverse chemoresistance by altering vital pathways like PI3K/AKT/ mTOR, MAPK/ERK, NF-κB, JAK/STAT, and Wnt/β-catenin. For example, quercetin inhibits NF-κB signalling and increases the cytotoxicity of doxorubicin, but curcumin decreases AKT phosphorylation. Furthermore, natural compounds may enhance immune response in BRCA-mutated TNBC by modifying immunological checkpoints, including PD-L1, when combined with PARP inhibitors.

conclusionNatural compounds are a promising supplementary method for TNBC therapy due to their ability to target unregulated pathways and overcome therapeutic resistance. Nevertheless, challenges such as pharmacokinetics, limited bioavailability, and a lack of clinical validation persist. Future research should focus on combinatorial regimens, nanocarrier-based delivery technologies, and biomarker-guided clinical trials to develop successful TNBC treatments.

Indexed as

Antineoplastic AgentsAntineoplastic Agents, PhytogenicBiological ProductsTriple Negative Breast NeoplasmsAnimalsCell ProliferationFemaleHumansAntineoplastic AgentsAntineoplastic Agents, PhytogenicBiological Productsbiomarkerclinical studiescurcuminsignaling pathwaystherapeutic strategiesTriple-negative breast cancer

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Registered trials

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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.