Evidence map›Paper›PMID 37024796›Full record

ArticleBMC cancer2023

Elemental profiles in distant tissues during tumor progression.

Samella Salles, Rebecca Salles, Mauro S G Pavão, Simone C Cardoso, Mariana P Stelling

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Ways to Measure Metals: From ICP-MS to XRF.Current environmental health reports · 2025
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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

5 authors at 3 institutions in 1 country.

Samella SallesFederal Institute of Education, Science and Technology of Rio de Janeiro (IFRJ), Rio de Janeiro, Brazil.
Rebecca SallesFederal Center of Technological Education (CEFET/RJ), Rio de Janeiro, Brazil.
Mauro S G PavãoMedical Biochemistry Institute, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
Simone C CardosoPhysics Institute, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
Mariana P StellingFederal Institute of Education, Science and Technology of Rio de Janeiro (IFRJ), Rio de Janeiro, Brazil. mariana.stelling@ifrj.edu.br.
Instituto Federal do Rio de Janeiro · BRUniversidade Federal do Rio de Janeiro · BRFederal Center for Technological Education of Minas Gerais · BR

Funding

Federal Institute of Education, Science and Technology of Rio de Janeiro Prociencia programFundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/101.407/2014
6 · The paper itself

Abstract

backgroundEssential elements have functions in tumor progression by promoting protumoral cellular processes, such as proliferation, and migration, among others. Obtaining an understanding of how these elements relate to tumor progression processes is of great importance for research. Elemental profile studies in distant tissues, which can be modulated by tumor cells to promote metastasis, have not been sufficiently investigated. The main goal of this study is to evaluate multielemental distribution during tumor progression, focusing on tumor tissue and distant tissues that may be affected.

methodsTumor progression in vivo was simulated by inoculating C57BL/6 mice with Lewis Lung Carcinoma (LLC) cells. Samples of the primary tumor and distant tissues were collected during 5 weeks of tumor progression for the control and experimental (tumor-bearing) groups. The biological samples were analyzed using the synchrotron radiation X-Ray fluorescence technique. Data on the concentration of P, S, K, Ca, Mn, Fe, Cu, and Zn in the samples were obtained and statistically analyzed to evaluate the distribution of the elements during tumor progression in the primary tumor as well as distant tissues.

resultsIt was possible to observe significant changes in the concentrations' distribution of P, S, K, Ca, Mn, Fe, and Cu in distant tissues caused by the presence of tumor cells. It was also possible to detect a greater similarity between tumor tissue (which has the lung as tissue of origin) and a tissue of non-origin, such as the liver, which is an unprecedented result. Moreover, changes in the distributions of concentrations were detected and studied over time for the different tissues analyzed, such as primary tumor, liver and lung, in Control and Tumor groups.

conclusionsAmong other results, this paper could explore the modulation of distant tissues caused by the presence of a primary tumor. This could be achieved by the evaluation of several elements of known biological importance allowing the study of different biological processes involved in cancer. The role of essential elements as modulators of the tumor microenvironment is a relevant aspect of tumor progression and this work is a contribution to the field of tumoral metallomics.

Indexed as

Neoplastic ProcessesTumor MicroenvironmentAnimalsMiceMice, Inbred C57BLElemental distributionEssential mineral elementsLewis lung carcinomaSR-XRFTumor progression

Identifiers

PMID37024796
PMCPMC10080929
OpenAlexW4362677255

What OpenQuestion holds

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LicenceCC BY
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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.