Evidence map›Paper›PMID 42324424›Full record

ArticleJournal of the Egyptian National Cancer Institute2026

Metformin enhances methylene blue-mediated photodynamic therapy in oral squamous cell carcinoma.

Mohamed A Osman, Marwa Sharaky, Hesham Abdel-Fattah, Ali M Safaan

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Article in Journal of the Egyptian National Cancer Institute, 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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5 · Who and what money

Authors and funding

4 authors.

Mohamed A OsmanDental Unit, Surgical Oncology Department, National Cancer Institute, Cairo University, Cairo, Egypt. std.mohamedosaman@niles.edu.eg.
Marwa SharakyCancer Biology Department, Pharmacology Unit, National Cancer Institute, Cairo University, Cairo, Egypt. marwa.sharaky@nci.cu.edu.eg.
Hesham Abdel-FattahDental Unit, Surgical Oncology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Ali M SafaanDepartment of Medical Application of Laser, National Institute of Laser Enhanced Sciences, Cairo University, Cairo, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHead and neck squamous cell carcinoma (HNSCC) is the most common malignancy of the head and neck region with relatively low survival rate and response and high resistance to treatment. Tongue and floor of the mouth are the most commonly involved sites. New therapies for oral squamous cell carcinoma (OSCC) treatment are still required. An attractive option for the treatment of OSCC is the use of photodynamic therapy (PDT). Considering metformin's potential to reduce cancer risk and inhibit proliferation, therefore the present study aims to evaluate its ability to potentiate the methylene blue-mediated photodynamic effect against the growth of tongue cancer cells in vitro and the possible molecular mechanisms of action involved.

methodsCytotoxic activity of metformin (MF) and/or Methylene blue (MB)+laser light (L) against the growth of HNO97 tongue cells was determined using the sulforhodamine (SRB) method. Several protein expressions were determined using ELISA kits include mechanistic target of rapamycin (mTOR), AMP-activated protein kinase (AMPK), B-cell lymphoma 2 (Bcl-2), Bcl-2-associated X protein (Bax), and caspase 8.

resultsLaser light at different energy per surface area induced inhibition in the surviving fraction of HNO97 cells, while in presence of MB (10 µg/ml for 4 h.), the surviving fractions showed more inhibition. Addition of MF (1000 µg/ml, for 24 h.) to MB + L induced significant 51 and 89% inhibition of cell survival at energy level of 45 and 337.5 J/cm

conclusionSuch combined treatment showed promising synergistic interaction via several molecular pathways, which is well tolerated and readily applicable strategy to improve the therapeutic outcome of PDT in cancer cell treatment.

Indexed as

Carcinoma, Squamous CellMetforminMethylene BlueMouth NeoplasmsPhotochemotherapyPhotosensitizing AgentsAMP-Activated Protein KinasesApoptosisCell Line, TumorCell ProliferationCell SurvivalHumansTOR Serine-Threonine KinasesAMP-Activated Protein KinasesMetforminMethylene BlueMTOR protein, humanPhotosensitizing AgentsTOR Serine-Threonine KinasesAMPKMetforminMethylene Blue-mediated PDTmTORTongue Squamous Cell Carcinoma

Identifiers

PMID42324424
PMCPMC13313284

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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.