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1.
Vaccines (Basel) ; 10(10)2022 Oct 16.
Article in English | MEDLINE | ID: mdl-36298592

ABSTRACT

One of the most effective cancer therapies, cancer immunotherapy has produced outstanding outcomes in the field of cancer treatment. However, the cost is excessive, which limits its applicability. A smart way to address this issue would be to apply the knowledge gained through immunotherapy to develop strategies for the immunoprevention of cancer. The use of cancer vaccines is one of the most popular methods of immunoprevention. This paper reviews the technologies and processes that support the advantages of cancer immunoprevention over traditional cancer immunotherapies. Nanoparticle drug delivery systems and nanoparticle-based nano-vaccines have been employed in the past for cancer immunotherapy. This paper outlines numerous immunoprevention strategies and how nanotechnology can be applied in immunoprevention. To comprehend the non-clinical and clinical evaluation of these cancer vaccines through clinical studies is essential for acceptance of the vaccines.

2.
Int J Colorectal Dis ; 37(7): 1509-1523, 2022 Jul.
Article in English | MEDLINE | ID: mdl-35704091

ABSTRACT

PURPOSE: Colorectal cancer (CRC) is the cancer of the colon and rectum. Recent research has found a link between CRC and human gut microbiota. This review explores the effect of gut microbiota on colorectal carcinogenesis and the development of chemoresistance. METHODS: A literature overview was performed to identify the gut microbiota species that showed altered abundance in CRC patients and the mechanisms by which some of them aid in the development of chemoresistance. RESULTS: Types of gut microbiota present and methods of analyzing them were discussed. We observed that numerous microbiota showed altered abundance in CRC patients and could act as a biomarker for CRC diagnosis and treatment. Further, it was demonstrated that microbes also have a role in the development of chemoresistance by mechanisms like immune system activation, drug modification, and autophagy modulation. Finally, the key issue of the growing global problem of antimicrobial resistance and its relationship with CRC was highlighted. CONCLUSION: This review discussed the role of gut microbiota dysbiosis on colorectal cancer progression and the development of chemoresistance.


Subject(s)
Colorectal Neoplasms , Gastrointestinal Microbiome , Microbiota , Colorectal Neoplasms/diagnosis , Dysbiosis/complications , Humans
3.
Biochem Biophys Res Commun ; 586: 14-19, 2022 01 01.
Article in English | MEDLINE | ID: mdl-34823217

ABSTRACT

Plakophilin3 (PKP3) loss leads to tumor progression and metastasis of colon cancer cells. The goal of this report was to determine if PKP3 loss led to increased disease progression in mice. We generated a colonocyte-specific knockout of PKP3 in APCmin mice, which led to increased adenoma formation, the formation of rectal prolapse, and a significant decrease in survival. The observed increase in rectal prolapse formation and decrease in survival correlated with an increase in the expression of Lipocalin2 (LCN2). Increased disease progression was observed even upon treatment with 5-fluorouracil (5FU). These results suggest that an increase in LCN2 expression might lead to therapy resistance and that LCN2 might serve as a potential therapeutic target in colorectal cancer.


Subject(s)
Adenoma/genetics , Colorectal Neoplasms/genetics , Drug Resistance, Neoplasm/genetics , Lipocalin-2/genetics , Plakophilins/genetics , Rectal Prolapse/genetics , Adenoma/drug therapy , Adenoma/mortality , Adenoma/pathology , Animals , Antimetabolites, Antineoplastic/pharmacology , Colon/drug effects , Colon/metabolism , Colon/pathology , Colorectal Neoplasms/drug therapy , Colorectal Neoplasms/mortality , Colorectal Neoplasms/pathology , Disease Progression , Female , Fluorouracil/pharmacology , Gene Expression Regulation, Neoplastic , Keratin-8/genetics , Keratin-8/metabolism , Lipocalin-2/metabolism , Male , Matrix Metalloproteinase 7/genetics , Matrix Metalloproteinase 7/metabolism , Mice , Mice, Inbred C57BL , Mice, Transgenic , Plakophilins/deficiency , Rectal Prolapse/drug therapy , Rectal Prolapse/mortality , Rectal Prolapse/pathology , Signal Transduction , Survival Analysis
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