Evidence map›Paper›PMID 38090376›Full record

ReviewAdvances in pharmacological and pharmaceutical sciences2023

Busting the Breast Cancer with AstraZeneca's Gefitinib.

S Chemmalar, A R Intan Shameha, Che Azurahanim Che Abdullah, Nor Asma Ab Razak, Loqman Mohamad Yusof, Mokrish Ajat, Kim Wei Chan, Md Zuki Abu Bakar Zakaria

Open access · goldAbstract readReview
In one paragraph

Review in Advances in pharmacological and pharmaceutical sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 22% of its field
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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

8 authors at 3 institutions in 2 countries.

S ChemmalarDepartment of Veterinary Anatomy, Veterinary College and Research Institute, Tamil Nadu Veterinary and Animal Sciences University (TANUVAS), Theni 625534, Tamil Nadu, India.ORCID https://orcid.org/0000-0003-3169-700X
A R Intan ShamehaDepartment of Veterinary Preclinical Sciences, Faculty of Veterinary Medicine, UPM, Serdang 43400, Selangor, Malaysia.ORCID https://orcid.org/0000-0001-6787-3621
Che Azurahanim Che AbdullahBiophysics Laboratory, Department of Physics, Faculty of Science, Laboratory of Cancer Research (MAKNA), Institute of Bioscience and Material Synthesis & Characterization Laboratory, Institute of Advanced Technology, UPM, Serdang 43400, Selangor, Malaysia.ORCID https://orcid.org/0000-0003-1023-3978
Nor Asma Ab RazakNatural Medicines and Products Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia (UPM), Serdang 43400, Selangor, Malaysia.ORCID https://orcid.org/0000-0002-3562-7052
Loqman Mohamad YusofDepartment of Companion Animal Medicine and Surgery, Faculty of Veterinary Medicine, UPM, Serdang 43400, Selangor, Malaysia.
Mokrish AjatDepartment of Veterinary Preclinical Sciences, Faculty of Veterinary Medicine and Natural Medicines and Product Research Laboratory, Institute of Bioscience, UPM, Serdang 43400, Selangor, Malaysia.ORCID https://orcid.org/0000-0002-2905-4630
Kim Wei ChanNatural Medicines and Products Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia (UPM), Serdang 43400, Selangor, Malaysia.ORCID https://orcid.org/0000-0003-3028-0800
Md Zuki Abu Bakar ZakariaNatural Medicines and Products Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia (UPM), Serdang 43400, Selangor, Malaysia.ORCID https://orcid.org/0000-0003-2152-5554
Universiti Putra Malaysia · MYSerdang Hospital · MYNational Cancer Council Malaysia · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the most common cancer diagnosed in women, and in 2020, there were 684, 996 deaths due to this disease. Epidermal growth factor receptors (EGFRs) and their respective ligands have been blamed for the pathogenesis and resistance to treatment in specific breast cancer cases. With EGFR having four homologues: EGFR1, EGFR2, EGFR3, and EGFR4, in-depth understanding of EGFR biology led to the discovery of small-molecule inhibitors and antibodies against this receptor. Gefitinib (GEF), a tyrosine kinase inhibitor of EGFR1, possesses a vast potential for treatment against breast cancer and is supported by a multiplicity of experiments. Unfortunately, in clinical trials, GEF did not show the outcomes expected with complete response and disease progress. This is due to incomplete understanding of the molecular mechanisms involved in EGFR signaling and endocrine sensitivity. Hence, additional in-depth experiments are needed regarding various molecular pathways and crosstalk pathways to comprehend GEF's action mechanism thoroughly in breast cancer patients. In this review, the role of EGFR in the development and pathogenesis of breast cancer and the pharmacokinetics and pharmacotherapy of GEF for the treatment of breast cancer have been elaborated. Nanomedicines synthesized with GEF have shown positive experimental response, paving a promising path for GEF against breast cancer.

Identifiers

PMID38090376
PMCPMC10713255
OpenAlexW4389297523

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.