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Immunotherapy: New Developments and Challenges

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Immunology".

Deadline for manuscript submissions: 20 January 2025 | Viewed by 2452

Special Issue Editors


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Guest Editor
Neher's Biophysics Laboratory for Innovative Drug Discovery, Macau University of Science and Technology, Macao, China
Interests: molecular pharmacology; cancer immunotherapy
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
School of Pharmacy, Macau University of Science and Technology, Macau 999078, China
Interests: infectious disease; malaria; virus; cancer; medicinal chemistry; natural compounds
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Immunotherapy is a promising strategy for cancer treatment that harnesses the power of the immune system to fight tumor cells. However, current immunotherapeutic agents have limitations such as high toxicity, low specificity, and poor bioavailability.

The most successful cancer therapies are immune checkpoint inhibitors (ICIs), bi-specific T-cell engagers (BiTEs), and chimeric antigen receptor T cells (CAR-T cells). The possibility for a combination therapy built on the aforementioned techniques has recently been considered by researchers and has been demonstrated to have a significantly stronger impact on cancer therapy. Therefore, new research methodologies are necessary for a full explanation of the processes behind various cancer therapeutic approaches.

This Special Issue aims to publish original research papers, systematic reviews, and opinion pieces that focus on clinical/translational cancer immunotherapy, covering both in vitro and in vivo experiments on new immunotherapeutic strategies, therapy-related immune regulation, and immunotherapy markers.

Dr. Xingxing Fan
Dr. Paolo Coghi
Guest Editors

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Keywords

  • tumor microenvironment
  • small molecules
  • IDO1 inhibition
  • checkpoint inhibitor therapy
  • adoptive T cell therapy
  • metabolic reprogram
  • resistance mechanisms
  • immune modulation
  • immune reconstitution
  • combination therapy
  • immunosuppression

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Published Papers (1 paper)

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Research

18 pages, 13605 KiB  
Article
The Transcriptional Landscape of Immune-Response 3′-UTR Alternative Polyadenylation in Melanoma
by Xiao Yang, Yingyi Wu, Xingyu Chen, Jiayue Qiu and Chen Huang
Int. J. Mol. Sci. 2024, 25(5), 3041; https://doi.org/10.3390/ijms25053041 - 6 Mar 2024
Viewed by 1795
Abstract
The prognosis of patients with malignant melanoma has been improved in recent decades due to advancements in immunotherapy. However, a considerable proportion of patients are refractory to treatment, particularly at advanced stages. This underscores the necessity of developing a new strategy to improve [...] Read more.
The prognosis of patients with malignant melanoma has been improved in recent decades due to advancements in immunotherapy. However, a considerable proportion of patients are refractory to treatment, particularly at advanced stages. This underscores the necessity of developing a new strategy to improve it. Alternative polyadenylation (APA), as a marker of crucial posttranscriptional regulation, has emerged as a major new type of epigenetic marker involved in tumorigenesis. However, the potential roles of APA in shaping the tumor microenvironment (TME) are largely unexplored. Herein, we collected two cohorts comprising melanoma patients who received immune checkpoint inhibitor (ICI) immunotherapy to quantify transcriptome-wide discrepancies in APA. We observed a global change in 3′-UTRs between responders and non-responders, which might involve DNA damage response, angiogenesis, PI3K-AKT signaling pathways, etc. Ten putative master APA regulatory factors for those APA events were detected via a network analysis. Notably, we established an immune response-related APA scoring system (IRAPAss), which exhibited a great performance of predicting immunotherapy response in multiple cohorts. Furthermore, we examined the correlation of APA with TME at the single-cell level using four single-cell immune profiles of tumor-infiltrating lymphocytes (TILs), which revealed an overall discrepancy in 3′-UTR length across diverse T cell populations, probably contributing to immunoregulation in melanoma. In conclusion, our study provides a transcriptional landscape of APA implicated in immunoregulation, which might lay the foundation for developing a new strategy for improving immunotherapy response for melanoma patients by targeting APA. Full article
(This article belongs to the Special Issue Immunotherapy: New Developments and Challenges)
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