Advances in Therapeutic Strategies and Precision Medicine in Solid Tumors and Metastasis—2nd Edition

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

Deadline for manuscript submissions: 30 September 2025 | Viewed by 374

Special Issue Editors


E-Mail Website
Guest Editor

E-Mail Website
Guest Editor
Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, Arcavacata di Rende, 87036 Cosenza, Italy
Interests: male reproduction; testicular cancer; prostate cancer
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

This Special Issue of Biomedicines is dedicated to showcasing the most innovative therapeutic strategies for the treatment of solid tumors.

Understanding molecular cancer pathogenesis has allowed scientists to develop increasingly effective treatment strategies. Over the last decade, whole-genome DNA sequencing technologies such as next-generation sequencing (NGS) have improved our genomic knowledge of several syndromes and diseases, including cancer. Furthermore, a multi-omics approach that also considers the analysis of the transcriptome, proteome, metabolome, and epigenetic DNA modifications could be transformative in better stratifying patients and providing further details on deregulated molecular pathways in tumors. Patients with a poor prognosis due to multiple mechanisms driving therapeutic resistance could also benefit from this multi-omics approach.

In some tumors, the use of personalized medicine throughout treatment, with monoclonal antibodies, immunotherapy, and epigenetic drugs, has already become a reality. In the future, the main objective will be to extend possible molecular targets so that even tumors with a high incidence of metastasis and mortality become more manageable through individualized anticancer therapies.

With this ambitious goal in mind, for this Special Issue, we welcome original research articles and reviews highlighting recent breakthroughs in personalized medicine and novel hypothetical targetable molecular mechanisms in cancer. We welcome contributions that employ robust molecular rationale to address topics in precision molecular therapy, nanodrug and molecule delivery, non-coding RNA-based therapeutics, and novel biomarkers that are useful in early diagnosis and prognosis.

Dr. Silvia Di Agostino
Dr. Vittoria Rago
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Biomedicines is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • kinase inhibitor
  • immunotherapy
  • chemotherapy
  • precision molecular therapy
  • biomarkers
  • synthetic lethality
  • theranostics
  • drug repurposing
  • radiomics

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • Reprint: MDPI Books provides the opportunity to republish successful Special Issues in book format, both online and in print.

Further information on MDPI's Special Issue policies can be found here.

Published Papers (1 paper)

Order results
Result details
Select all
Export citation of selected articles as:

Research

25 pages, 12425 KiB  
Article
DBI as a Novel Immunotherapeutic Candidate in Colorectal Cancer: Dissecting Genetic Risk and the Immune Landscape via GWAS, eQTL, and pQTL
by Ting Tian, Huan Han, Jingtao Huang, Jun’e Ma and Ruoxi Ran
Biomedicines 2025, 13(5), 1115; https://doi.org/10.3390/biomedicines13051115 - 4 May 2025
Viewed by 230
Abstract
Background: Colorectal cancer (CRC) is a leading cause of cancer-related mortality worldwide. Identifying drug targets associated with CRC is crucial for developing targeted therapies. Methods: MR (IVW, Wald ratio, weighted median, and MR-Egger) and SMR analyses were used to screen candidate genes associated [...] Read more.
Background: Colorectal cancer (CRC) is a leading cause of cancer-related mortality worldwide. Identifying drug targets associated with CRC is crucial for developing targeted therapies. Methods: MR (IVW, Wald ratio, weighted median, and MR-Egger) and SMR analyses were used to screen candidate genes associated with CRC risk. Further validation was performed using The Cancer Genome Atlas (TCGA) to assess gene expression patterns and prognostic significance. Additionally, immune infiltration analysis was conducted to characterize the tumor immune microenvironment. Drug prediction was performed to explore potential therapeutic interventions. Results: Eight genes were identified associated with CRC. IGFBP3, CD72, SERPINH1, CHRDL2, LRP11, and SPARCL1 were linked to an increased risk of CRC, whereas DBI and HYAL1 were associated with a decreased risk of CRC. Notably, DBI exhibited a potentially favorable immune profile, negatively correlated with Tregs and MDSCs while positively associated with activated CD8+ and CD4+ T cells. Conclusions: Eight genes were identified as associated with CRC, among which DBI exhibited a potential protective role, correlating with improved patient survival, enhanced immune activation, and increased responsiveness to immunotherapy. The remaining proteins demonstrated diverse and complex functions within the tumor immune microenvironment, providing novel insights for the development of precision diagnostics and immunotherapeutic strategies. Full article
Show Figures

Figure 1

Back to TopTop