Molecular Research on Pancreatic Cancer: Current Trends and New Perspectives

A special issue of Biomedicines (ISSN 2227-9059). This special issue belongs to the section "Cancer Biology and Oncology".

Deadline for manuscript submissions: closed (30 September 2023) | Viewed by 1238

Special Issue Editors


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Guest Editor
Faculty of Medicine and Surgery, Fondazione Policlinico Universitario Agostino Gemelli IRCCS Università Cattolica del Sacro Cuore, 00168 Rome, Italy
Interests: pancreatic cancer; biliary tract cancer; cancerogenesis; drug resistance; molecular pathway; microenvironment; tumor molecular profile; precision medicine

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Guest Editor
1.Fondazione Policlinico Universitario Agostino Gemelli IRCCS Università Cattolica del Sacro Cuore, 00168 Rome, Italy
2.Medical Oncology, Università Cattolica del Sacro Cuore, 00168 Rome, Italy
Interests: pancreatic cancer; hepatobiliary cancer; microenvironment; cancerogenesis; translational research; biomarkers

Special Issue Information

Dear Colleagues,

Over the last decade we observed a significant improvement in the prognosis of many solid tumors thanks to the advent of immunotherapy and targeted therapies expanding the therapeutic opportunities for cancer patients and realizing the promise of personalized medicine. Despite these advances, pancreatic cancer remains an incurable disease, where immune-checkpoint inhibitors and targeted drugs are generally not efficacious. For this reason, it is still perceived as a hopeless disease by both patients and physicians. More than 80% of pancreatic cancer patients are diagnosed when the tumor is in contact with vascular structures or when distant metastases are present, and thus surgical excision is not indicated. For these patients, the standard of care is palliative chemotherapy, with a median overall survival of 11 months. Since 2011, three independent studies by Collison, Moffit and Bailey identified different pancreatic cancer subtypes based on gene expression profiles, suggesting that pancreatic cancer is not a unique entity, but should be regarded as a collection of different diseases. As demonstrated for other cancers, the identification of molecular subtypes allows a better prediction of disease behavior and the design of targeted therapeutic strategies. This Special Issue addresses the molecular and clinical heterogeneity of pancreatic cancer, presenting studies regarding molecular pathways involved in pancreatic cancer development, metastasization and treatment resistance, thus suggesting potential therapeutic strategies for more personalized and effective therapy.

Dr. Cinzia Bagalà
Dr. Marta Chiaravalli
Guest Editors

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Keywords

  • pancreatic cancer
  • tumor growth
  • metastatization
  • microenvironment
  • drug resistance
  • molecular pathway
  • targeted therapy
  • immunotherapy
  • tumor molecular profile
  • precision medicine

Published Papers (1 paper)

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Research

16 pages, 3145 KiB  
Article
MiR-506 Promotes Antitumor Immune Response in Pancreatic Cancer by Reprogramming Tumor-Associated Macrophages toward an M1 Phenotype
by Tiantian Yang, Yitong Han, Junhang Chen, Xiaoyu Liang and Longhao Sun
Biomedicines 2023, 11(11), 2874; https://doi.org/10.3390/biomedicines11112874 - 24 Oct 2023
Cited by 1 | Viewed by 882
Abstract
Pancreatic ductal adenocarcinoma (PDAC) is a highly malignant cancer with a poor prognosis, and effective treatments for PDAC are lacking. In this study, we hypothesized that miR-506 promotes antitumor immune response in PDAC by reprogramming tumor-associated macrophages toward an M1 phenotype to reverse [...] Read more.
Pancreatic ductal adenocarcinoma (PDAC) is a highly malignant cancer with a poor prognosis, and effective treatments for PDAC are lacking. In this study, we hypothesized that miR-506 promotes antitumor immune response in PDAC by reprogramming tumor-associated macrophages toward an M1 phenotype to reverse its immunosuppressive tumor microenvironment (TME). First, the relationship between TME and the expression of miR-506 was assessed using clinical samples. Our results provided evidence that lower expression of miR-506 was associated with poor prognosis and immunosuppressive TME in PDAC patients. In addition, miR-506 inhibit the PDAC progression and reversed its immunosuppressive microenvironment in a macrophage-dependent manner. Next, we established a PDAC mouse model by orthotopic injection to further explore the role of miR-506 in vivo. Mechanistic investigations demonstrated that miR-506 could reprogram the polarization of M2-like macrophages toward an M1-like phenotype through targeting STAT3. Meanwhile, miR-506 could also sensitize PDAC to anti-PD-1 immunotherapy, because the tumor microenvironment remodeling effects of miR-506 could reprogram macrophage polarization and subsequently promote cytotoxic T lymphocyte (CTL) infiltration. These findings suggest a relationship between miR-506 and TME, especially M2-like macrophages, thus providing novel insights into mechanisms of tumor progression and potential immunotherapeutic targets for further clinical treatment. Full article
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