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Esophageal basaloid squamous cell carcinoma (EBSCC) is a rare subtype of esophageal squamous cell carcinoma (ESCC) that might be misdiagnosed or missed in clinical practice. Through RNA sequencing on 20 pure EBSCC and 11 poorly differentiated ESCC samples, we identified CSPG4 as a potential marker for EBSCC at the mRNA level, and verified with CSPG4 immunohistochemical staining in these cases. Then we assessed the value of CSPG4 expression in differential diagnosis and prognosis in EBSCC cases (n = 360) and conventional ESCC cases (n = 160) from 11 different institutions with whole-tissue sections. CSPG4 had acceptable discriminatory capacity for EBSCC, with an AUC ROC of 0.891. The optimal cutoff value for the H-score determined by ROC curve analysis was 77.5, with 82.7% sensitivity and 79.9% specificity. In well-moderately differentiated ESCC with CSPG4 expression, staining was mostly observed on the edge of the tumor nest or infiltration front, with different expression pattern from EBSCC. The H-scores of CSPG4 expression for the EBSCC component were higher than those for other components in the same tissue section (P < 0.05). The expression level of CSPG4 was similar in groups with different percentages of the EBSCC component (P > 0.05). In additional 505 ESCC patients, patients with high CSPG4 expression had decreased DFS and OS, especially in stage I-II disease (P < 0.001). The similar prognostic significance was also found in EBSCC. Our data indicate that CSPG4 is not only a sensitive but also a specific marker for the diagnosis of EBSCC. CSPG4 might also be a prognostic marker for ESCC.
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http://dx.doi.org/10.1007/s00428-024-04020-2 | DOI Listing |
Ann Med
December 2025
Department of Urology, The Second Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, People's Republic of China.
Background: Bladder cancer (BLCA) is a prevalent malignancy with substantial consequences for patient health. This study aimed to elucidate the underlying mechanisms of BLCA through integrated multi-omics analysis.
Methods: Tumor and adjacent tissues from BLCA patients underwent transcriptomic, whole-exome sequencing, metabolomic, and intratumoral microbiome analyses.
While significant progress has been made in understanding the heterogeneity in the NSCs, our understanding of similar heterogeneity among the more abundant transit amplifying progenitors is lagging. Our work on the NPs of the neonatal subventricular zone (SVZ) began over a decade ago, when we used antibodies to the 4 antigens, Lex CD133,LeX,CD140a and NG2 and FACs to classify subsets of the neontal SVZ as either multi-potential (MP1, MP2, MP3, MP4 and PFMPs), glial-restricted (GRP1, GRP2, and GRP3), or neuron-astrocyte restricted (BNAP). Using RNAseq we have characterized the distinctive molecular fingerprint of 4 SVZ neural progenitors and compared their gene expression profiles to those of the NSCs.
View Article and Find Full Text PDFJ Exp Clin Cancer Res
August 2025
Department of Surgery, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Background: Anaplastic thyroid cancer (ATC) is a rare and aggressive malignancy with poor survival and no available effective therapy. This unmet clinical need led us to investigate chimeric antigen receptor (CAR) T cells s as potential treatment option for this malignant disease. As target tumor antigens of our CAR T cell therapy, we selected the chondroitin sulfate proteoglycan 4 (CSPG4) and the B7-homolog 3 (B7-H3), as they are both highly and homogeneously expressed on different types of thyroid carcinoma cell lines and tissues, including ATC.
View Article and Find Full Text PDFAnim Sci J
August 2025
Laboratory of Veterinary Physiology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.
Skeletal muscle regeneration is a complex process that requires coordinated interactions between myogenic and vascular cells. Chondroitin sulfate proteoglycan 4 (CSPG4), a cell surface proteoglycan, had been shown to be expressed around immature myofibers in patients with Duchenne muscular dystrophy, suggesting its role in muscle regeneration. In the present study, we found that CSPG4 is transiently expressed by regenerating myofibers upon muscle injury in the rat.
View Article and Find Full Text PDFCells
July 2025
Department of Plastic and Reconstructive Surgery, Cell and Matrix Research Institute, School of Medicine, Kyungpook National University, Kyungpook National University Hospital, Daegu 41944, Republic of Korea.
Arteriovenous malformations (AVMs) are congenital vascular anomalies defined by abnormal direct connections between arteries and veins due to their complex structure or endovascular approaches. Pharmacological strategies targeting the underlying molecular mechanisms are thus gaining increasing attention in an effort to determine the mechanism involved in AVM regulation. In this study, we examined 30 human tissue samples, comprising 10 vascular samples, 10 human fibroblasts derived from AVM tissue, and 10 vascular samples derived from healthy individuals.
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