Evidence map›Paper›PMID 35405370›Full record

ArticleMolecular metabolism2022

Metformin overcomes metabolic reprogramming-induced resistance of skin squamous cell carcinoma to photodynamic therapy.

Marta Mascaraque-Checa, María Gallego-Rentero, Jimena Nicolás-Morala, Mikel Portillo-Esnaola, José M Cuezva, Salvador González, Yolanda Gilaberte, Ángeles Juarranz

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

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  15. Modulating Glycolysis to Improve Cancer Therapy.International journal of molecular sciences · 2023
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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 4 institutions in 1 country.

Marta Mascaraque-ChecaDepartament of Biology, Universidad Autónoma de Madrid, Madrid, Spain; Instituto Ramón y Cajal de Investigaciones Sanitarias, IRYCIS, Madrid, Spain.
María Gallego-RenteroDepartament of Biology, Universidad Autónoma de Madrid, Madrid, Spain; Instituto Ramón y Cajal de Investigaciones Sanitarias, IRYCIS, Madrid, Spain.
Jimena Nicolás-MoralaDepartament of Biology, Universidad Autónoma de Madrid, Madrid, Spain; Instituto Ramón y Cajal de Investigaciones Sanitarias, IRYCIS, Madrid, Spain.
Mikel Portillo-EsnaolaDepartament of Biology, Universidad Autónoma de Madrid, Madrid, Spain; Instituto Ramón y Cajal de Investigaciones Sanitarias, IRYCIS, Madrid, Spain.
José M CuezvaCentro de Biología Molecular-Severo Ochoa (CBMSO/CSIC) and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER-ISCIII), Universidad Autónoma de Madrid, Madrid, Spain.
Salvador GonzálezDepartment of Medicine and Medical Specialties, Universidad de Alcalá, Madrid, Spain.
Yolanda GilaberteDepartament of Dermatología, Hospital Miguel Servet, Zaragoza, Spain.
Ángeles JuarranzDepartament of Biology, Universidad Autónoma de Madrid, Madrid, Spain; Instituto Ramón y Cajal de Investigaciones Sanitarias, IRYCIS, Madrid, Spain. Electronic address: angeles.juarranz@uam.es.
Instituto Ramón y Cajal de Investigación Sanitaria · ESHospital Universitario Miguel Servet · ESInstituto de Salud Carlos III · ESUniversidad de Alcalá · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCancer metabolic reprogramming promotes resistance to therapies. In this study, we addressed the role of the Warburg effect in the resistance to photodynamic therapy (PDT) in skin squamous cell carcinoma (sSCC). Furthermore, we assessed the effect of metformin treatment, an antidiabetic type II drug that modulates metabolism, as adjuvant to PDT.

methodsFor that, we have used two human SCC cell lines: SCC13 and A431, called parental (P) and from these cell lines we have generated the corresponding PDT resistant cells (10GT).

resultsHere, we show that 10GT cells induced metabolic reprogramming to an enhanced aerobic glycolysis and reduced activity of oxidative phosphorylation, which could influence the response to PDT. This result was also confirmed in P and 10GT SCC13 tumors developed in mice. The treatment with metformin caused a reduction in aerobic glycolysis and an increase in oxidative phosphorylation in 10GT sSCC cells. Finally, the combination of metformin with PDT improved the cytotoxic effects on P and 10GT cells. The combined treatment induced an increase in the protoporphyrin IX production, in the reactive oxygen species generation and in the AMPK expression and produced the inhibition of AKT/mTOR pathway. The greater efficacy of combined treatments was also seen in vivo, in xenografts of P and 10GT SCC13 cells.

conclusionsAltogether, our results reveal that PDT resistance implies, at least partially, a metabolic reprogramming towards aerobic glycolysis that is prevented by metformin treatment. Therefore, metformin may constitute an excellent adjuvant for PDT in sSCC.

Indexed as

Antineoplastic AgentsCarcinoma, Squamous CellMetforminPhotochemotherapyAnimalsCell Line, TumorHumansMiceAntineoplastic AgentsMetforminAKT/mTOR pathwayCancer resistanceMetforminPhotodynamic therapySkin squamous cell carcinomaWarburg effect

Identifiers

PMID35405370
PMCPMC9048115
OpenAlexW4223542607

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.