Genetic and Molecular Mechanisms of Cardiometabolic Diseases and Cancers—2nd Edition

A special issue of Biomedicines (ISSN 2227-9059). This special issue belongs to the section "Molecular Genetics and Genetic Diseases".

Deadline for manuscript submissions: 31 December 2025 | Viewed by 1042

Special Issue Editors


E-Mail Website
Guest Editor
Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China
Interests: genetic epidemiology; cardiometabolic disease
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China
Interests: molecular epidemiology of chronic diseases; data mining
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Cardiometabolic diseases (CMDs) and cancers, the two most prevalent non-communicable diseases globally, constitute major concerns worldwide. Recent evidence suggests close co-morbid linkages and shared risk factors between CMDs and cancers, calling for an integrated and systematic interrogation into their intercorrelation. Nevertheless, the mechanisms whereby genetic and other factors contribute to their co-occurrence remain unclear. Further research is therefore expected to provide novel insights into the genetic and molecular mechanisms underlying their correlations. Possible perspectives may involve shared genetic factors like genetic pleiotropy. In addition, complex interactions between genes and the environment, such as inter-generational genetic and environment transmission and interacting phenotypes influenced by genotypes, as well as their effects on the differentiated co-morbidity risks, require more comprehensive assessment.

In this Special Issue, we intend to take CMDs and cancers as examples to elucidate the intricate interconnections among complex diseases, and we welcome the submission of original high-quality research and review articles focused on (1) disease comorbidities; (2) genetic pleiotropy and heterogeneity; (3) genetic overlap and causality between CMD and cancers; and (4) indirect genetic effects.

Prof. Dr. Tao Wu
Prof. Dr. Dafang Chen
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

  • cardiometabolic disease
  • oncology
  • comorbidity
  • genetic pleiotropy
  • direct genetic effects
  • indirect genetic effects
  • parent-of-origin

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.

Related Special Issue

Published Papers (1 paper)

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

Research

18 pages, 7538 KiB  
Article
Genetic Nurture Effects on Type 2 Diabetes Among Chinese Han Adults: A Family-Based Design
by Xiaoyi Li, Zechen Zhou, Yujia Ma, Kexin Ding, Han Xiao, Tao Wu, Dafang Chen and Yiqun Wu
Biomedicines 2025, 13(1), 120; https://doi.org/10.3390/biomedicines13010120 - 7 Jan 2025
Viewed by 805
Abstract
Background/Objectives: Genes and environments were transmitted across generations. Parents’ genetics influence the environments of their offspring; these two modes of inheritance can produce a genetic nurture effect, also known as indirect genetic effects. Such indirect effects may partly account for estimated genetic [...] Read more.
Background/Objectives: Genes and environments were transmitted across generations. Parents’ genetics influence the environments of their offspring; these two modes of inheritance can produce a genetic nurture effect, also known as indirect genetic effects. Such indirect effects may partly account for estimated genetic variance in T2D. However, the well-established specific genetic risk factors about genetic nurture effect for T2D are not fully understood. This study aimed to investigate the genetic nurture effect on type 2 diabetes and reveal the potential underlying mechanism using publicly available data. Methods: Whole-genome genotyping data of 881 offspring and/or their parents were collected. We assessed SNP-level, gene-based, and pathway-based associations for different types of genetic effects. Results: Rs3805116 (β: 0.54, p = 4.39 × 10−8) was significant for paternal genetic nurture effects. MRPS33 (p = 1.58 × 10−6), PIH1D2 (p = 6.76 × 10−7), and SD1HD (p = 2.67 × 10−6) revealed significantly positive paternal genetic nurture effects. Five ontologies were identified as enrichment in both direct and indirect genetic effects, including flavonoid metabolic process and antigen processing and presentation via the MHC class Ib pathway. Two pathways were only enriched in paternal genetic nurture effects, including the transforming growth factor beta pathway. Tissue enrichment of type 2 diabetes-associated genes on different genetic effect types was performed using publicly available gene expression data from the Human Protein Atlas database. We observed significant gene enrichment in paternal genetic nurture effects in the gallbladder, smooth muscle, and adrenal gland tissues. Conclusions: MRPS33, PIH1D2, and SD1HD are associated with increased T2D risk through the environment influenced by paternal genotype, suggesting a novel perspective on paternal contributions to the T2D predisposition. Full article
Show Figures

Figure 1

Back to TopTop