Evidence map›Paper›PMID 42730982›Full record

ArticleMolecular biology reports2026

Proteomic regulation of anti-proliferative and anti-migratory activity by potent phytochemicals from Pistacia integerrima J.L. Steward Ex Brandis via PI3K, AKT1, and KRAS for Lung Cancer.

Anshul Jamwal, Keshav Paudel, Kamal Dua, Mangesh Pradeep Kulkarni, Somdutt Mujwar, Sunny Dhiman, Vikrant Dalwal, Poonam Negi, Rohit Goyal

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Anshul JamwalSchool of Pharmaceutical Sciences, Shoolini University, 173229, HP, Bajhol, Solan, India.
Keshav PaudelNICM Health Research Institute, School of Science, Western Sydney University, Westmead, NSW, 2145, Australia.
Kamal DuaNICM Health Research Institute, School of Science, Western Sydney University, Westmead, NSW, 2145, Australia.
Mangesh Pradeep KulkarniDiscipline of Pharmacy, Graduate School of Health, University of Technology Sydney, Sydney, NSW, 2007, Australia.
Somdutt MujwarChitkara College of Pharmacy, Chitkara University, Rajpura, 140401, Punjab, India.ORCID https://orcid.org/0000-0003-4037-5475
Sunny DhimanDepartment of Pharmacology, Shanti Niketan College of Pharmacy, Mandi, 175008, HP, India.
Vikrant DalwalDepartment of Pharmaceutical Chemistry, Gautam College of Pharmacy, Hamirpur, 177001, H.P, India.ORCID https://orcid.org/0009-0001-5132-502X
Poonam NegiAmity Institute of Pharmacy, Amity University of Punjab, Sector 82A, Mohali, 140306, Mohali, India. poonamgarge@gmail.com.
Rohit GoyalSchool of Pharmaceutical Sciences, Shoolini University, 173229, HP, Bajhol, Solan, India. rohitgoyal@shooliniuniversity.com.ORCID http://orcid.org/0000-0001-6307-0055

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNon-small cell lung cancer (NSCLC) is the leading cause of mortality worldwide and remains a major therapeutic challenge due to high metastasis, drug resistance and limited treatments. Pistacia integerrima J.L. Steward Ex Brandis (PI) consists of flavonoids, steroids, terpenoids and phenolic compounds reported for pharmacological activities. The efficacy of potent bioactives from P. integerrima may be ascertained employing cytotoxic, antiproliferative, anti-migratory, and anti-metastatic evaluations in A549 NSCLC cells with proteomic profiling, molecular docking, and dynamics simulation study. METHODS AND

resultsPI EtAc produced significant dose-dependent cytotoxicity in A549 cells (100 µg/mL, p < 0.0001 in the MTT assay. There was a pronounced decrease in colony formation after treatment with EtAc, with 18.41% (p < 0.002), and markedly. Furthermore. PI EtAC markedly inhibited cell migration emphasized by wound healing and Transwell migration (p < 0.01) assays, indicating reduced metastatic migratory potential. Proteomic analysis demonstrated significant downregulation of Endoglin (CD105), KLK5 and MMP-2, indicating suppression of angiogenic and metastatic signalling pathways in the Human XL Oncology protein array. The interaction of major PI phytochemicals with key NSCLC-associated targets was recorded in Molecular docking, revealing favourable binding affinities of kaempferol, β- sitosterol, luteolin, and quercetin towards several oncogenic targets, including AKT1(- 7.6 kcal/mol), PI3K(- 9.4 kcal/mol), KRAS (- 8.5 kcal/mol) and MMP9 (- 8.1 kcal/mol). Molecular dynamics simulation confirmed the structural stability of the kaempferol -AKT1 complex throughout the 100 ns simulation.

conclusionPistacia integerrima bioactives exhibited significant anti-proliferative, anti-migratory, and anti-metastatic activities in vitro, which may provide scientific rationale identifying newer promising candidates for NSCLC.

Indexed as

Lung NeoplasmsPhytochemicalsPistaciaA549 CellsCarcinoma, Non-Small-Cell LungCell Line, TumorCell MovementCell ProliferationHumansMolecular Docking SimulationPhosphatidylinositol 3-KinasesPlant ExtractsProteomicsProto-Oncogene Proteins c-aktProto-Oncogene Proteins p21(ras)Signal TransductionAKT1 protein, humanKRAS protein, humanPhosphatidylinositol 3-KinasesPhytochemicalsPlant ExtractsProto-Oncogene Proteins c-aktProto-Oncogene Proteins p21(ras)A549 cellsFlavonoidsKRASmolecular dockingNon-small cell lung cancerPI3K/AKT1 signallingPistacia integerrima

Identifiers

PMID42730982

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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.