Publications by authors named "Ruhao Zhou"

Chondrosarcoma is 1 of the most common malignant bone tumors, with dedicated research being conducted by scientists worldwide. The purpose of this study was to guide researchers in identifying valuable scholars, institutions, and countries, provide recommendations for journal submissions, and explore research trends and hotspots in chondrosarcoma studies through literature analysis. Data for this study were collected from the Web of Science Core Collection website.

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Article Synopsis
  • Previous research has linked gut microbiota (GM) and their metabolites to various cancers, but few studies have explored their connection to osteosarcoma (OS).
  • This study created an osteosarcoma mouse model to analyze the GM and metabolites, revealing dysregulation in amino acid metabolism associated with OS.
  • The results suggest that understanding the relationship between GM and OS could lead to improved therapeutic and diagnostic approaches, addressing the ineffectiveness of current treatment methods like surgery and chemotherapy.
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Micro RNAs (miRs) have been implicated in various tumorigenic processes. Osteosarcoma (OS) is a primary bone malignancy seen in adolescents. However, the mechanism of miRs in OS has not been fully demonstrated yet.

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Background: The gut microbiota (GM) constitutes a critical factor in the maintenance of physiological homeostasis. Numerous studies have empirically demonstrated that the GM is closely associated with the onset and progression of osteoporosis (OP). Nevertheless, the characteristics of the GM and its metabolites related to different forms of OP are poorly understood.

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The gut microbiota is closely associated with tumor progression and treatment in a variety of cancers. However, the alteration of the gut microbiota during the progression and chemotherapy of osteosarcoma remains poorly understood. This study aimed to explore the relationship between dysbiosis in the gut microbiota during osteosarcoma growth and chemotherapy treatment.

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Metabolic reprogramming is one of the cancer hallmarks, important for the survival of malignant cells. We investigated the prognostic value of genes associated with metabolism in thyroid carcinoma (THCA). A prognostic risk model of metabolism-related genes (MRGs) was built and tested based on datasets in The Cancer Genome Atlas (TCGA), with univariate Cox regression analysis, LASSO, and multivariate Cox regression analysis.

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Article Synopsis
  • Research shows that gut microbiota (GM) is linked to bone health, with dysbiosis (imbalance) potentially impacting bone metabolism, especially in disuse-induced osteoporosis (DIO).
  • In a study using rat models, significant changes in GM and fecal metabolites were observed in DIO subjects compared to controls, highlighting altered bile acid metabolism and specific bacteria associated with bone health.
  • The findings suggest that changes in GM and fecal metabolites may contribute to DIO-related bone loss, indicating a need for further exploration of their regulatory roles in this condition.
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Background: Recently, increasing attention has been drawn to the impact of the tumor microenvironment (TME) on the occurrence and progression of malignant tumors. A variety of 3D culture techniques have been used to simulate TME in vitro. The purpose of this study was to reveal the differences in transcriptional and metabolic levels between osteosarcoma (OS) 2D cells, 3D cells, 3D cell-printed tissue, isolated tissue, and transplanted tumor tissue in vivo.

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Background: Silencing of the periostin gene (POSTN) can inhibit the biological process of several different cancers, and this inhibition may be related to down-regulation of PI3K/AKT signaling. However, the effect of POSTN on the progression, proliferation, and invasion of osteosarcoma (OS) remain unclear.

Methods: We used the Gene Expression Omnibus (GEO) database to screen datasets on in situ OS and lung metastases to identify core genes and potential pathways.

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