The Mechanisms or Targets by Which the Microbiome Inhibits or Enhances Anti-inflammation or Tumor

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cellular Pathology".

Deadline for manuscript submissions: closed (30 September 2024) | Viewed by 1548

Special Issue Editor


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Guest Editor
1. Division of Hematology and Oncology, Department of Medicine MetroHealth Medical Center (MHMC), Case Western Reserve University (CWRU), School of Medicine, Cleveland, OH 10900, USA
2. Division of Cancer Biology, Department of Medicine MetroHealth Medical Center (MHMC), Case Western Reserve University (CWRU), School of Medicine, Cleveland, OH 10900, USA
Interests: gut mucosal immunology; epithelial barrier repair; inflammatory bowel diseases; colorectal cancer; intestinal epithelial and stem cell pathophysiology
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Special Issue Information

Dear Colleagues,

Background and Aims: Mounting evidence demonstrates that the gut microbiome is required for maintaining gut epithelial integrity, anti-inflammation or anti-tumor immunity, and systemic metabolism homeostasis. Shifts in gut microbial composition have been found to play a causal role in chronic mucosal inflammation and colon cancer. However, a lack of studies on the mechanisms or signaling pathways by which the microbiome acts on the host limits the development of microbiota treatments. Therefore, the Aim of this Special Issue is to promote basic and applied research that will identify the strains of gut beneficial or pathological bacteria and their metabolic products, with a particular emphasis on the mechanisms or targets by which the microbiota inhibits or enhances anti-inflammation or tumor.

Scope

  1. Gut microbiomeand epithelial integrity. In this part, the Special Issue is interested in by which signaling pathways the strains of gut commensal bacteria protect epithelial barriers from inflammation or pathogens.
  2. Gut microbiomeand anti-inflammation. In this part, the Special Issue is interested in the mechanics of the reduced Bifidobacterium and Lactobacillus in inflammatory bowel diseases (IBDs).
  3. Gut microbiome and anti-tumor. In this part, the Special Issue is interested in the signaling pathways by which the patients with a higher presence of Fusobacterium nucleatum or other validated onco-bacteria are prone to colon cancer.
  4. Gut microbiome and protective immune responses. It was recently shown that a subset of microbe-induced intestinal Th17 cells do not provoke intestinal inflammation. In this part, the Special Issue is interested in how specific gut microbiota promote host protective immune responses in cancer prevention.
  5. Gut microbiomeand immune tolerance. In this part, the Special Issue is interested in the effects of gut bacteria on the secretion of cytokines (e.g., IL-10), growth factor (e.g., TGF) and Treg cells that are able to suppress the inflammatory responses caused by microbiota-derived antigens in the gut.
  6. Gut microbiome and systemic metabolism homeostasis. In this part, the Special Issue is interested in how short-chain fatty acid production from microbiota affects anti-tumor immune functions, as well as examining how microbial bile acid metabolism modulates immune responses in colon tumors.

Dr. Xiaonan Han
Guest Editor

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Keywords

  • microbiome
  • IBD
  • colon cancer
  • colitis-associated cancer
  • Th17 cells
  • cytokines
  • immune tolerance

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Published Papers (1 paper)

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Review

47 pages, 1728 KiB  
Review
Microbiota and Resveratrol: How Are They Linked to Osteoporosis?
by Christine Meyer, Aranka Brockmueller, Vicenç Ruiz de Porras and Mehdi Shakibaei
Cells 2024, 13(13), 1145; https://doi.org/10.3390/cells13131145 - 3 Jul 2024
Cited by 1 | Viewed by 1063
Abstract
Osteoporosis (OP), which is characterized by a decrease in bone density and increased susceptibility to fractures, is closely linked to the gut microbiota (GM). It is increasingly realized that the GM plays a key role in the maintenance of the functioning of multiple [...] Read more.
Osteoporosis (OP), which is characterized by a decrease in bone density and increased susceptibility to fractures, is closely linked to the gut microbiota (GM). It is increasingly realized that the GM plays a key role in the maintenance of the functioning of multiple organs, including bone, by producing bioactive metabolites such as short-chain fatty acids (SCFA). Consequently, imbalances in the GM, referred to as dysbiosis, have been identified with a significant reduction in beneficial metabolites, such as decreased SCFA associated with increased chronic inflammatory processes, including the activation of NF-κB at the epigenetic level, which is recognized as the main cause of many chronic diseases, including OP. Furthermore, regular or long-term medications such as antibiotics and many non-antibiotics such as proton pump inhibitors, chemotherapy, and NSAIDs, have been found to contribute to the development of dysbiosis, highlighting an urgent need for new treatment approaches. A promising preventive and adjuvant approach is to combat dysbiosis with natural polyphenols such as resveratrol, which have prebiotic functions and ensure an optimal microenvironment for beneficial GM. Resveratrol offers a range of benefits, including anti-inflammatory, anti-oxidant, analgesic, and prebiotic effects. In particular, the GM has been shown to convert resveratrol, into highly metabolically active molecules with even more potent beneficial properties, supporting a synergistic polyphenol–GM axis. This review addresses the question of how the GM can enhance the effects of resveratrol and how resveratrol, as an epigenetic modulator, can promote the growth and diversity of beneficial GM, thus providing important insights for the prevention and co-treatment of OP. Full article
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