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Drug resistance biomarkers in ovarian cancer: a bibliometric study from 2017 to 2022
Indexado
WoS WOS:001362817100001
Scopus SCOPUS_ID:85210095312
DOI 10.3389/FONC.2024.1450675
Año 2024
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



Background: Late diagnosis and patient relapse, mainly due to chemoresistance, are the key reasons for the high mortality rate of ovarian cancer patients. Hence, the search for biomarkers of high predictive value within the phenomenon of chemoresistance is vital. This study performs a bibliometric analysis of the scientific literature concerning biomarkers of drug resistance in ovarian cancer, considering the period from 2017 to 2022. Methods: The terms "drug resistance biomarker" and "ovarian cancer" were linked by the Boolean operator "AND". The search was done in PubMed, selecting documents published over the last 5 years (2017-2022), which were analyzed with the open-source tool Bibliometrix developed in the R package. The language of the publications was restricted to English. Several types of papers such as case reports, clinical trials, comparative studies, and original articles were considered. Results: A total of 335 scientific articles were analyzed. The United States and China were the leading contributors and established the largest number of scientific collaborations. The Huazhong University of Science and Technology and the University of Texas MD Anderson Cancer Center were the most influential institutions. The Journal of Ovarian Research, International Journal of Molecular Science, and Scientific Reports are among the most relevant journals. The study identified high-profile, relevant thematic niches and important descriptors that indicate topics of interest, including studies on women, cell lines, solid tumors, and gene expression regulation. As well as studies involving middle-aged and adult participants, and those focusing on prognosis evaluation. Descriptors such as "drug resistance," "neoplasm," "genetics," "biomarker," "gene expression profile," and "drug therapy" would indicate new research trends. In addition, we propose that BCL-2, CHRF, SNAIL, miR-363, iASPP, ALDH1, Fzd7, and EZH2 are potential biomarkers of drug resistance. Conclusions: This paper contributes to the global analysis of the scientific investigation related to drug resistance biomarkers in ovarian cancer to facilitate further studies and collaborative networks, which may lead to future improvements in therapy for this lethal disease.

Revista



Revista ISSN
Frontiers In Oncology 2234-943X

Métricas Externas



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Disciplinas de Investigación



WOS
Oncology
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



Ord. Autor Género Institución - País
1 Cabarca, Sindy - Universidad de La Frontera - Chile
Univ Sucre - Colombia
Universidad de Sucre - Colombia
2 Ili, Carmen - Universidad de La Frontera - Chile
3 Vanegas, Carlos - Univ Sucre - Colombia
Universidad de Sucre - Colombia
4 Gil, Laura - Univ Sucre - Colombia
Univ Cauca - Colombia
Universidad de Sucre - Colombia
Universidad del Cauca - Colombia
5 Vertel-Morrinson, Melba - Univ Sucre - Colombia
UNIV CORDOBA - Colombia
Universidad de Sucre - Colombia
Universidad de Córdoba, Monteria - Colombia
6 Brebi, Priscilla - Universidad de La Frontera - Chile

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Financiamiento



Fuente
FONDECYT
Fondo Nacional de Desarrollo Científico y Tecnológico
FONDEF IdeA
Postdoctoral Fondecyt Projects
Agencia Nacional de Investigación y Desarrollo
Agencia Nacional de Investigacion y Desarrollo (ANID)- Millennium Science Initiative Program

Muestra la fuente de financiamiento declarada en la publicación.

Agradecimientos



Agradecimiento
The author(s) declare fi nancial support was received for the research, authorship, and/or publication of this article. Agencia Nacional de Investigacion y Desarrollo (ANID)- Millennium Science Initiative Program- ICN09_016/ICN 2021_045: Millennium Institute on Immunology and Immunotherapy (ICN09_016/ICN 2021_045; formerly P09/016-F). POSTDOCTORAL FONDECYT PROJECTS N degrees 3220156 FONDEF Idea N degrees ID21I10027 and FONDECYT 1210440.
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. Agencia Nacional de Investigaci\u00F3n y Desarrollo (ANID) - Millennium Science Initiative Program - ICN09_016/ICN 2021_045: Millennium Institute on Immunology and Immunotherapy (ICN09_016/ICN 2021_045; formerly P09/016-F). POSTDOCTORAL FONDECYT PROJECTS N\u00B0 3220156 FONDEF Idea N\u00B0 ID21I10027 and FONDECYT 1210440.

Muestra la fuente de financiamiento declarada en la publicación.