Second Edition of Advances in Adipose Tissue Biology

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Tissues and Organs".

Deadline for manuscript submissions: 20 November 2025 | Viewed by 1059

Special Issue Editor


E-Mail Website
Guest Editor
1. Department of Endocrinology, Division of Medicine, Tan Tock Seng Hospital, Singapore 308433, Singapore
2. Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore 636921, Singapore
3. Singapore Institute for Clinical Sciences, Brenner Centre for Molecular Medicine, Agency for Science, Technology and Research (A*STAR), Singapore 117609, Singapore
4. Cardiovascular and Metabolic Disorders Program, Duke-NUS Medical School, Singapore 169857, Singapore
5. Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Singapore
Interests: adipocyte biology; metabolic syndrome/diabetes; thyroidology; endocrine manifestations of systemic disorders; mathematical modeling of endocrine physiology
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

This Special Issue is the second edition of “Advances in Adipose Tissue Biology” https://www.mdpi.com/journal/cells/special_issues/Adipose_Tissue_Biology.

Much progress in the past two decades has revolutionized our understanding of adipose tissues in the body. Fat is no longer simply thought of as a homogeneous organ that shields the body from cold and mechanical shocks. Once believed to be an inert fat depot with few biological properties, recent advances facilitated by cutting-edge ‘omics’ and other novel scientific methodologies have probed and elucidated the pleiotropic nature of this organ at the molecular level. Even its role in fat storage can predispose adipose tissue toward pathological trajectories; new evidence supports fat expandability defects and ectopic fat deposition as drivers of metabolic disease. Apart from regulating triglyceride energy storage, adipocytes secrete numerous bioactive cargoes housed within extracellular vesicles, released from their cell membranes into the circulation, thereby exerting a broad range of distant endocrine effects elsewhere in the body. In addition, the plasticity of adipocytes has implications in remodeling and tissue engineering for obesity treatment aimed at the browning of white adipose tissues. We now appreciate how heterogeneity existing within adipose tissues orchestrates complex dynamics, signaling, and feedbacks in the maintenance of health and disease. Notably, adipocytes have been demonstrated to act as stromal cells in the tumor microenvironment, with molecular crosstalk having been proven to promote cancer-cell proliferation, migration, invasion, and metastasis. The disruption of adipocyte homeostasis caused by both genes and the environment with consequent metabolic dysfunction contributes to system-wide inflammation that underlies many non-communicable chronic disease pandemics, such as non-alcoholic fatty liver disease, obesity, diabetes, cardiovascular diseases, and even cancers.

The study of adipose biology has thus entered a new era. In this respect, this Special Issue aims to showcase scientific advances and fascinating discoveries that may not only be translated to the bedside and address the burgeoning toll exacted by obesity, diabetes, and the like, but also further propel both basic scientists and clinical researchers to greater breakthroughs. Toward that end, the articles in this Special Issue will hopefully serve as an inspiring resource for all who wish to have up-to-date knowledge concerning this most fascinating biological field.

Prof. Dr. Melvin K. S. Leow
Guest Editor

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. Cells is an international peer-reviewed open access semimonthly 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 2700 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

  • adipocyte differentiation, progenitors, and stem cells
  • adipokines, myokines, hepatokines, cytokines, cellular signaling, and molecular crosstalk
  • white adipose tissue (WAT) and brown adipose tissue (BAT)
  • beige fat and browning of WAT
  • research techniques and methodologies
  • diagnostics and therapeutics, genomics, metabolomics, other ‘omics’ technologies
  • metabolic syndrome, obesity, insulin resistance, cancer

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.
  • e-Book format: Special Issues with more than 10 articles can be published as dedicated e-books, ensuring wide and rapid dissemination.

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

Related Special Issue

Published Papers (1 paper)

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

Research

14 pages, 2225 KiB  
Article
Supplementation with Fish Oil and Selenium Protects Lipolytic and Thermogenic Depletion of Adipose in Cachectic Mice Treated with an EGFR Inhibitor
by Hang Wang, Yi-Lin Chan, Yi-Han Chiu, Tsung-Han Wu, Simon Hsia and Chang-Jer Wu
Cells 2024, 13(17), 1485; https://doi.org/10.3390/cells13171485 - 4 Sep 2024
Viewed by 904
Abstract
Lung cancer and cachexia are the leading causes of cancer-related deaths worldwide. Cachexia is manifested by weight loss and white adipose tissue (WAT) atrophy. Limited nutritional supplements are conducive to lung cancer patients, whereas the underlying mechanisms are poorly understood. In this study, [...] Read more.
Lung cancer and cachexia are the leading causes of cancer-related deaths worldwide. Cachexia is manifested by weight loss and white adipose tissue (WAT) atrophy. Limited nutritional supplements are conducive to lung cancer patients, whereas the underlying mechanisms are poorly understood. In this study, we used a murine cancer cachexia model to investigate the effects of a nutritional formula (NuF) rich in fish oil and selenium yeast as an adjuvant to enhance the drug efficacy of an EGFR inhibitor (Tarceva). In contrast to the healthy control, tumor-bearing mice exhibited severe cachexia symptoms, including tissue wasting, hypoalbuminemia, and a lower food efficiency ratio. Experimentally, Tarceva reduced pEGFR and HIF-1α expression. NuF decreased the expression of pEGFR and HIF-2α, suggesting that Tarceva and NuF act differently in prohibiting tumor growth and subsequent metastasis. NuF blocked LLC tumor-induced PTHrP and expression of thermogenic factor UCP1 and lipolytic enzymes (ATGL and HSL) in WAT. NuF attenuated tumor progression, inhibited PTHrP-induced adipose tissue browning, and maintained adipose tissue integrity by modulating heat shock protein (HSP) 72. Added together, Tarceva in synergy with NuF favorably improves cancer cachexia as well as drug efficacy. Full article
(This article belongs to the Special Issue Second Edition of Advances in Adipose Tissue Biology)
Show Figures

Figure 1

Back to TopTop