1.Expression of the Transmembrane Glycoprotein CD44s Is Potentially an Independent Predictor of Recurrence in Hepatocellular Carcinoma.
Han Suk RYU ; Sun Hoo PARK ; Kyung Bun LEE ; Eun SHIN ; Ja June JANG
Gut and Liver 2011;5(2):204-209
BACKGROUND/AIMS: Cluster differentiation 44 standard isoform (CD44s) is a transmembrane glycoprotein. CD44s is a known prognostic factor in various cancers, due to its involvement in tumor cell growth, invasion and metastasis. Its prognostic role, however, is debated because it can be a positive or negative prognostic factor depending on tumor type and is still an ambiguous prognostic indicator in other cancers, especially hepatocellular carcinoma (HCC). We investigated the relationship between CD44s expression and survival in HCC patients. METHODS: A total of 260 HCC samples were collected to generate a tissue microarray. Staining of the arrays with a primary mouse CD44s monoclonal antibody was followed by evaluation of the relationship between CD44s expression and tumor differentiation. The effect of CD44s expression on patient survival was analyzed. RESULTS: CD44s protein expression correlated with histological grade (most and worst Edmondson grade) of the HCC (p=0.029 and p=0.039, respectively) and adversely affected the disease free survival period based on univariate and multivariate analyses (p=0.038 and p=0.077, respectively). CONCLUSIONS: High CD44s protein expression correlates with shorter disease free survival and poorly differentiated HCC. CD44s-targeted therapy may be efficacious for HCC treatment in the future.
Animals
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Antigens, CD44
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Carcinoma, Hepatocellular
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Disease-Free Survival
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Glycoproteins
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Humans
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Mice
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Multivariate Analysis
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Neoplasm Metastasis
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Protein Array Analysis
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Recurrence
2.Biological characteristics of human bone marrow mesenchymal stem cell cultured in vitro.
Xian'en, FA ; Lixia, WANG ; Jianfeng, HOU ; Ruicheng, ZHANG ; Haiyong, WANG ; Chenyuan, YANG
Journal of Huazhong University of Science and Technology (Medical Sciences) 2005;25(3):307-9
Some biological characteristics of human bone marrow mesenchymal stem cells (MSCs) cultured in vitro were observed. hMSCs were isolated from bone marrow and purified by density gradient centrifugation method, and then cultured in vitro. The proliferation and growth characteristics of hMSCs were observed in primary and passage culture. MSCs of passage 3 were examined for the purify by positive rate of CD29 and CD44 through flow cytometry. Human bone marrow MSCs showed active proliferation capacity in vitro. The purify of MSCs separated by our method was higher than 90%. It was concluded that hMSCs have been successfully cultured and expanded effectively. It provided a foundation for further investigation and application of MSCs.
Antigens, CD29/analysis
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Antigens, CD44/analysis
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Bone Marrow Cells/*cytology
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Cell Proliferation
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Cell Separation
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Cells, Cultured
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Flow Cytometry
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Mesenchymal Stem Cells/*cytology
3.CD44 and MMP14 Expression Associated with WHO Grade of the Astrocytoma and the Prognostic Implications.
Jaekyung MYUNG ; Bogun JANG ; Heae Surng PARK ; Woongjae YON ; Hyun Ju LEE ; Sung Hye PARK
Korean Journal of Pathology 2010;44(1):35-41
BACKGROUND: CD44 is a cell surface receptor that has been implicated in tumor cell invasion and metastasis in a range of tumors of various organs, including breast, ovary, colon, lung, and brain. CD44 stimulates the invasive ability by interacting with matrix metalloproteinase 14 (MMP14). The expression of MMP14 on the cell surface is thought to trigger multiple proteinase cascades and to stimulate cell migration. METHODS: A total 54 astrocytoma patients were eligible for this study. We performed a retrospective clinicopathological review and CD44 and MMP14 immunohistochemistry. RESULTS: The expressions of CD44 and MMP14 were significantly correlated with the World Health Organization (WHO) grade. On univariate analysis, the WHO grade and the expression of CD44 were the significant prognostic factors affecting overall survival (OS) and disease progression free survival (DPFS). On the multivariate analysis by the Cox regression model, the only WHO grade was shown to be a significant independent prognostic factor for predicting the DPFS and OS. CONCLUSIONS: In this study, the CD44 and MMP14 expressions were related to the WHO grade of astrocytoma. The CD44 expression status was a prognostic factor for DPFS and OS on univariate analysis, but it was not an independent prognostic factor on the multivariate analysis.
Antigens, CD44
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Astrocytoma
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Brain
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Breast
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Colon
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Disease Progression
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Female
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Humans
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Lung
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Matrix Metalloproteinase 14
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Multivariate Analysis
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Neoplasm Metastasis
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Ovary
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Prognosis
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Retrospective Studies
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World Health Organization
4.Expression of CD44 Isoforms and Its Significance in Renal Cell Carcinoma.
Ghil Suk YOON ; Hee Yeon HONG ; Tae Sook KIM
Korean Journal of Pathology 2005;39(4):251-257
Background : CD44 is a transmembranous glycoprotein that participates in cell-cell and cell-matrix interactions, and it also contributes to cell migration. In vitro studies have suggested that the expression of CD44 isoforms is associated with tumor metastasis. Since it is not clear whether the CD44 isoforms play a role in the tumorigenesis, differentiation, progression or metastasis of renal cell carcinomas (RCCs). Methods : We performed immunohistochemistry with primary antibodies for the standard CD44 (CD44s) and the CD44 variant exon 6 (CD44v6) on the archival paraffin-embedded tissue microarray (TMA) specimens from 51 RCC patients. Results : In the normal kidney, the expressions of both CD44s and CD44v6 were negligible. The CD44s expression was increased in accordance with the tumor size (p<0.01), but it was not related to the microvessel density (MVD). No CD44v6 expression was observed in all RCC cases. Univariate analysis indicated that stage, tumor size, lymph node metastasis and distant organ metastasis were the statistically significant prognostic factors for disease free survival (DFS) (p<0.01), and the multivariate analysis proved that stage (p<0.01) and tumor size (p<0.05) were the independent prognostic factors for DFS. Conclusions : Our results suggest that CD44s, but not CD44v6, plays a role in tumor progression and it could be a potential prognostic factor for patients with RCCs.
Antibodies
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Antigens, CD44
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Carcinogenesis
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Carcinoma, Renal Cell*
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Cell Movement
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Disease-Free Survival
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Exons
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Glycoproteins
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Humans
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Immunohistochemistry
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Kidney
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Lymph Nodes
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Microvessels
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Multivariate Analysis
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Neoplasm Metastasis
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Protein Isoforms*
5.Identification of CD44 splice variant in Korean colorectal cancers and cell lines.
Seong Il SUH ; Won Ki BAEK ; Jong Wook PARK ; Ok Suk BAE ; Min Ho SUH ; Byung Kil CHOE
Journal of Korean Medical Science 1995;10(3):169-175
CD44 is a glycoprotein expressed in a wide variety of cell types. Recently expression of some alternatively-spliced variants of CD44 transcripts (CD44v) has been suggested to play a potential role in tumor metastasis and the detection of CD44v containing exon 6 to 11 may be helpful for the diagnosis of cancers. Expressions of CD44v containing exon 6 to 11 were investigated in 20 human colorectal cancer samples, peripheral blood leukocytes isolated from colorectal cancer patients, and 4 colorectal cancer cell lines using reverse transcription-polymerase chain reaction and Southern blot analysis. The standard form of CD44 transcripts was expressed in all samples tested. CD44v containing exon 6 to 11 was expressed in 18 cases of colorectal cancers (sensitivity = 90%), 3 out of 4 cell lines, and one normal tissue (specificity = 95%). These results suggest that the expression of CD44v containing exon 6 to 11 can be regarded as tumor specific and that this marker may be helpful for the early diagnosis of colon cancers, if specimens from the early stage are available.
Adenocarcinoma/*genetics
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Adult
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Aged
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Antigens, CD44/*genetics
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Base Sequence
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Blotting, Southern
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Colorectal Neoplasms/diagnosis/*genetics
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DNA Primers
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Electrophoresis, Agar Gel
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Feces/chemistry/cytology
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Female
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Gene Expression Regulation, Neoplastic/genetics
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Human
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Male
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Middle Age
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Molecular Sequence Data
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Polymerase Chain Reaction
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RNA Splicing/*physiology
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RNA, Messenger/analysis
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Tumor Cells, Cultured/*physiology
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Tumor Markers, Biological
6.Detection of Malignant Cells in Pleural Fluid or Ascites by CD44v8-10/CD44v10 competitive RT-PCR.
Myung Ju AHN ; Yun Hee NOH ; Ho Ju YOON ; Suck Cheol YANG ; Jang Won SOHN ; Jung Hae CHOI ; Young Yeul LEE ; Il Young CHOI ; In Soon KIM ; Yong Sung LEE ; Chan Kum PARK
The Korean Journal of Internal Medicine 2001;16(1):30-35
BACKGROUND: CD44 is a cell surface adhesion molecule which has been implicated in various biologic functions as lymphocyte homing and activation, cellular migration and extracellular matrix adhesion. Over-expression of CD44v8- 10 has been found in several cancers and is considered to be associated with tumor progression and metastasis. Recently, a novel molecular method, CD44v8- 10/CD44v10 competitive reverse transcription-polymerase chain reaction(RT-PCR) has been developed for detecting cancer cells over-expressing CD44v8-10. METHODS: We analyzed from benign and malignant pleural effusion and ascites by CD44 competitive RT-PCR and compared to the conventional cytology. RESULTS: The CD44 competitive RT-PCR analysis showed that all the 24 samples associated with benign disease presented a predominant expression of the CD44v10 transcript (v8-10/v10 ratio: 0.126-0.948), whereas 6 of 7 malignant pleural samples associated with cytology positive cancer expressed the CD44v8-10 transcript (v8-10/v10 ratio > 1.00). CONCLUSION: These results indicate that CD44 competitive RT-PCR assay is a useful and adjunct to cytological examination in cancer diagnosis, especially in detecting exfoliated cancer cells in pleural effusion.
Adult
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Aged
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Aged, 80 and over
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Antigens, CD44/analysis*
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Ascites/pathology*
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Ascites/immunology*
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Base Sequence
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Carcinoma, Non-Small-Cell Lung/pathology
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Carcinoma, Non-Small-Cell Lung/immunology
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Comparative Study
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Female
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Gastrointestinal Neoplasms/pathology
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Gastrointestinal Neoplasms/immunology
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Human
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Lung Neoplasms/pathology
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Lung Neoplasms/chemistry
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Male
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Middle Age
;
Molecular Sequence Data
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Pleural Effusion, Malignant/pathology*
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Pleural Effusion, Malignant/chemistry*
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Reverse Transcriptase Polymerase Chain Reaction*
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Sensitivity and Specificity
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Support, Non-U.S. Gov't