98%
921
2 minutes
20
In our daily life, our skin is frequently exposed to water, which can affect human health. Previous studies have demonstrated that water bathing improves skin conditions in individuals with dermatoses. However, whether groundwater bathing influences epidermal gene expression in normal skin is largely unknown. Therefore, we compared epidermal gene expression in mice exposed in groundwater and deionized water. Flank of mouse skin was exposed to either groundwater or deionized water for 30 min twice daily for three consecutive days. Expression levels of epidermal mRNA were compared between the skin exposed to deionized and groundwaters. In comparison to deionized water, spring water A (Yichun) upregulated 257 genes and downregulated 380 genes, while spring water B (AVENE) upregulated 242 genes and downregulated 668 genes. Moreover, spring water A upregulated 469 genes and downregulated 277 genes compared to spring water B. Spring water A downregulated genes were mainly enriched in the pathways associated with keratinization, keratinocyte differentiation and development, while upregulated genes were enriched in the pathways associated with muscle contraction, sarcomere organization and skeletal muscle fiber development. Whereas genes upregulated by spring water B were associated with pathways related to ion transport and activation of endothelial cells, while downregulated genes were related to keratinization, response to bacteria and keratinocyte differentiation. Collectively, groundwater can affect epidermal gene expression. The influences of water bathing on epidermal gene expression vary with water, likely due to the differences in active constitutes in the water. However, the clinical significance of altered epidermal gene expression remains to be explored.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.ecoenv.2025.118545 | DOI Listing |
Appl Immunohistochem Mol Morphol
September 2025
Department of Pathology, Yantai Yuhuangding Hospital of Qingdao University, Yantai, P. R. China.
To investigate the clinicopathological characteristics of non-HPV-related common differentiated penile squamous cell carcinoma, and to observe and analyze the changes of TP53 gene and the expression and significance of TP53, P16, programmed death-ligand 1 (PD-L1), epidermal growth factor receptor (EGFR), androgen receptor (AR), human epidermal growth factor receptor-2 (HER2), and Ki67 proteins in tumor tissue. A total of 65 patients with penile squamous cell carcinoma diagnosed from May 2008 to May 2020 in Yantai Yuhuangding Hospital were retrospectively analyzed, and tumors were confirmed as non-HPV-associated common differentiated squamous cell carcinoma of the penis with negative HPV molecular tests in 55 patients. The relevant clinicopathological data of 55 patients were collected, and the TP53 gene mutation was detected by applying first-generation sequencing technology.
View Article and Find Full Text PDFCell Genom
September 2025
Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Breast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA, USA; Harvard Medical School, Boston, MA, USA.
Though there has been substantial progress in the development of anti-human epidermal growth factor receptor 2 (HER2) therapies to treat HER2-positive metastatic breast cancer (MBC) within the past two decades, most patients still experience disease progression and cancer-related death. HER2-directed tyrosine kinase inhibitors can be highly effective therapies for patients with HER2-positive MBC; however, an understanding of resistance mechanisms is needed to better inform treatment approaches. We performed whole-exome sequencing on 111 patients with 73 tumor biopsies and 120 cell-free DNA samples to assess mechanisms of resistance.
View Article and Find Full Text PDFEcotoxicol Environ Saf
September 2025
College of Environment and Climate, Guangdong Key Laboratory of Environmental Pollution and Health, Jinan University, Guangzhou, Guangdong 510632, China.
Synthetic antioxidants and plasticizers have emerged as environmental contaminants to which prenatal exposure is widespread, raising concerns about adverse pregnancy outcomes. This study aimed to investigate the association between prenatal exposure to a mixture of synthetic antioxidants and plasticizers and the risk of spontaneous preterm birth (SPB), alongside underlying molecular responses. A nested case-control design was established, including 80 SPB cases and 170 matched healthy controls.
View Article and Find Full Text PDFPathol Res Pract
September 2025
Department of Pathology, Xijing Hospital and School of Basic Medicine, Fourth Military Medical University, Xi'an, China. Electronic address:
Background: Dermal clear cell sarcoma (DCCS) is a rare malignant mesenchymal neoplasm. Owing to the overlaps in its morphological and immunophenotypic profiles with a broad spectrum of tumors exhibiting melanocytic differentiation, it is frequently misdiagnosed as other tumor entities in clinical practice. By systematically analyzing the clinicopathological characteristics, immunophenotypic features, and molecular biological properties of DCCS, this study intends to further enhance pathologists' understanding of this disease and provide a valuable reference for its accurate diagnosis.
View Article and Find Full Text PDFBiochem Biophys Rep
December 2025
Division of Breast Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei, 112, Taiwan.
Purpose: This study aimed to conduct functional proteomics across breast cancer subtypes with bioinformatics analyses.
Methods: Candidate proteins were identified using nanoscale liquid chromatography with tandem mass spectrometry (NanoLC-MS/MS) from core needle biopsy samples of early stage (0-III) breast cancers, followed by external validation with public domain gene-expression datasets (TCGA TARGET GTEx and TCGA BRCA).
Results: Seventeen proteins demonstrated significantly differential expression and protein-protein interaction (PPI) found the strong networks including COL2A1, COL11A1, COL6A1, COL6A2, THBS1 and LUM.