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Global trends in resistance studies of gemcitabine and pancreatic cancer: a bibliometric and visual analysis from 2010 to 2024.

作者信息

Gu Dandan, Huang Shaoyang, Zhao Kai, Zhang Xiaohong, Zhang Jinjing, Xiong Wei

机构信息

Department of Gastroenterology, Northeast Yunnan Regional Central Hospital, Zhaotong, China.

College of Life Sciences, Shaanxi Normal University, Xi'an, China.

出版信息

Front Pharmacol. 2025 Apr 25;16:1564561. doi: 10.3389/fphar.2025.1564561. eCollection 2025.


DOI:10.3389/fphar.2025.1564561
PMID:40351434
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12062017/
Abstract

INTRODUCTION: Pancreatic adenocarcinoma (PC) represents a prevalent and highly aggressive malignancy within the digestive system, characterized by an exceedingly poor prognosis and a dismal 5-year survival rate of below 7%. Gemcitabine (GEM) remains the cornerstone chemotherapeutic agent in the management of PC; however, the growing challenge of GEM chemoresistance, which undermines treatment efficacy, represents a significant obstacle in clinical practice. To date, no comprehensive bibliometric analysis has been undertaken to systematically explore studies on GEM resistance in the context of PC. This study aims to deliver a thorough evaluation of the research hotspots pertaining to GEM resistance in PCs. METHOD: A systematic search was conducted for articles published from 1 January 2010, to 15 December 2024, focusing on resistance studies of GEM in PC. Bibliometric analysis and visualization were performed utilizing VOSviewer and CiteSpace tools, applied to literature data extracted from the Web of Science Core Collection (WoSCC). RESULTS: Between 2010 and 2024, a total of 2,689 papers were published across 472 institutions in 74 countries, reflecting a consistent upward trajectory in annual publication output. China and Fudan University emerged as the leading contributors to the research output on this topic, representing the most prolific country and institution, respectively. Giovannetti, Elisa, and Yu, Xianjun are the most prolific scholars in this field. stands out as the most cited and impactful journal, while research on the tumor microenvironment, targeted therapy, and circular RNA has emerged as a key focus area in recent years. CONCLUSION: This study provides a systematic and comprehensive overview of the literature on GEM resistance in PC over the past 15 years. This analysis offers scholars critical insights into the field from a bibliometric perspective, potentially informing future studies on the development of chemotherapeutic treatments for PC.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/d3000f48cc25/fphar-16-1564561-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/b2479d3c3c8b/fphar-16-1564561-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/eade31585ad3/fphar-16-1564561-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/030af50b93d5/fphar-16-1564561-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/0f0e33dff36a/fphar-16-1564561-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/f52484270a4c/fphar-16-1564561-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/d3000f48cc25/fphar-16-1564561-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/b2479d3c3c8b/fphar-16-1564561-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/eade31585ad3/fphar-16-1564561-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/030af50b93d5/fphar-16-1564561-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/0f0e33dff36a/fphar-16-1564561-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/f52484270a4c/fphar-16-1564561-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e58/12062017/d3000f48cc25/fphar-16-1564561-g006.jpg

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Global trends in resistance studies of gemcitabine and pancreatic cancer: a bibliometric and visual analysis from 2010 to 2024.

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本文引用的文献

[1]
Glycolysis reprogramming in CAFs promotes oxaliplatin resistance in pancreatic cancer through circABCC4 mediated PKM2 nuclear translocation.

Cell Death Dis. 2025-2-23

[2]
Precision medicine for pancreatic cancer: characterizing the clinicogenomic landscape and outcomes of KRAS G12C-mutated disease.

J Natl Cancer Inst. 2024-9-1

[3]
Cancer statistics, 2024.

CA Cancer J Clin. 2024

[4]
Pancreatic cancer: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up.

Ann Oncol. 2023-11

[5]
T Cell Exhaustion and Activation Markers in Pancreatic Cancer: A Systematic Review.

J Gastrointest Cancer. 2024-3

[6]
Pancreatic cancer: Advances and challenges.

Cell. 2023-4-13

[7]
Global research trends between gut microbiota and lung cancer from 2011 to 2022: A bibliometric and visualization analysis.

Front Oncol. 2023-2-23

[8]
First-in-Human Study of OBI-999, a Globo H-Targeting Antibody-Drug Conjugate, in Patients With Advanced Solid Tumors.

JCO Precis Oncol. 2023-1

[9]
Induction of pancreatic neoplasia in the KRAS/TP53 Oncopig.

Dis Model Mech. 2023-1-1

[10]
Barriers and opportunities for gemcitabine in pancreatic cancer therapy.

Am J Physiol Cell Physiol. 2023-2-1

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