1.Research Advances in Chemokine-like Factor Super Family Member 8.
Deng-Hui GAO ; Hao HU ; Zhi-Wei FANG ; Fei HUO ; Huan-Rui WANG ; Ke-Xin XU ; Xiao-Feng WANG
Acta Academiae Medicinae Sinicae 2016;38(6):746-749
Chemokine-like factor super family member (CMTM) is a novel generic family firstly reported by Peking University Center for Human Disease Genomics. CMTM8 is one member of this family and has exhibited tumor-inhibiting activities. It can encode proteins approaching to the transmembrane 4 superfamily. CMTM8 is down-regulated in most carcinoma cell lines and tissues. Over-expression of CMTM8 may inhibit the proliferation,migration,and invasion of carcinoma cells. However,the exact mechanism of its anti-tumor activity remains unclear. CMTM8 may be involved in various signaling pathways governing the occurrence and development of tumors. CMTM8 may be a new target in the gene therapies for tumors,while further studies on CMTM8 and its anti-tumor mechanisms are warranted.
Chemokines
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metabolism
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Down-Regulation
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Humans
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MARVEL Domain-Containing Proteins
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metabolism
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Neoplasms
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metabolism
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Signal Transduction
3.Research advances in CKLF-like MARVEL transmembrane domain containing member 5.
Ye-qing YUAN ; Yun-bei XIAO ; Zhen-hua LIU ; Xiao-wei ZHANG ; Tao XU ; Xiao-feng WANG
Acta Academiae Medicinae Sinicae 2012;34(6):625-628
CKLF-like MARVEL transmembrane domain containing member(CMTM)is a novel generic family firstly reported by Peking University Center for Human Disease Genomics. CMTM5 belongs to this family and has exhibited tumor-inhibiting activities. It can encode proteins approaching to the transmembrane 4 superfamily(TM4SF). CMTM5 is broadly expressed in normal adult and fetal human tissues, but is undetectable or down-regulated in most carcinoma cell lines and tissues. Restoration of CMTM5 may inhibit the proliferation, migration, and invasion of carcinoma cells. Although the exact mechanism of its anti-tumor activity remains unclear, CMTM5 may be involved in various signaling pathways governing the occurrence and development of tumors. CMTM5 may be a new target in the gene therapies for tumors, while further studies on CMTM5 and its anti-tumor mechanisms are warranted.
Chemokines
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genetics
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metabolism
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Humans
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MARVEL Domain-Containing Proteins
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genetics
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metabolism
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Neoplasms
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genetics
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metabolism
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Signal Transduction
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Tumor Suppressor Proteins
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genetics
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metabolism
4.The expression of CEACAM-1 and CXCL-14 in infantile hemangioma.
Guang-Qi XU ; Ren-Rong LÜ ; Ran HUO ; Xuan GUO
Chinese Journal of Plastic Surgery 2010;26(3):195-198
OBJECTIVETo examine the expression of CEACAM-land CXCL-14 in the different stages of infantile hemangioma and to explore the role of CEACAM-1 and CXCL-14 in the occurrence and development of infantile hemangioma.
METHODSThe expression of CEACAM-1 and CXCL-14 was detected by immunohistochemical technique and Western Blot in cases of proliferating hemangiomas, involuting hemangiomas, involuted hemangiomas. The mean optical density was measured by image analysis system.
RESULTSThe expression of CEACAM-1 in early stage of proliferating hemangiomas was weak or negative, while it was strong in involuting hemangiomas and positive in the involuted stage. The differences between different stages had a statistically significance (P < 0.05). The expression of CXCL-14 was weak or negative in stage of proliferating hemangiomas, positive in involuting hemangiomas and strong in the involuted stage. The differences between different stages had a statistically significance (P < 0.05).
CONCLUSIONSCEACAM-1 and CXCL-14 are involved in the occurrence and development of infantile hemangioma.
Antigens, CD ; metabolism ; Cell Adhesion Molecules ; metabolism ; Chemokines, CXC ; metabolism ; Child ; Child, Preschool ; Female ; Hemangioma ; metabolism ; pathology ; Humans ; Infant ; Male
6.Progress of studies on microenvironment of lymphoma.
Journal of Experimental Hematology 2011;19(5):1310-1313
Many studies indicate that lymphoid neoplasms are related with chromosome translocations and the molecular alterations involving in the cell cycle and/or apoptotic pathways. However, survival of B and T tumor cells also depends on interactions of these cells with the accompanying cells comprising the lymphoma microenvironment. Immune cells, stromal cells and numerous molecular together make up the microenvironment and have functional interaction with tumor cells, promoting tumor growth and drug resistance. Different types of lymphoma have various clinical courses, therapy responses and prognoses, which show a close relationship with the microenvironment. This review summarizes several components of lymphoma microenvironment including macrophages, adhesion molecules and chemokines and the roles of microenvironment in classic non-Hodgkin's lymphoma, follicular lymphoma, diffuse large B-cell lymphoma, suggesting that the microenvironment influence the prognosis of lymphoma, targeting microenvironment may be a potential method in lymphoma therapy.
Apoptosis
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Cell Adhesion Molecules
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Cell Cycle
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Chemokines
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Humans
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Lymphoma
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metabolism
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pathology
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Macrophages
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Tumor Microenvironment
7.Cumulation and effect of chemokines and CD40L during blood storage--review.
Journal of Experimental Hematology 2010;18(5):1350-1353
Chemokine is a class of soluble active peptides that attract white blood cells to the inflammatory site. CD40 ligand (CD40L) involves in synthesis of proinflammatory mediators. Accumulation of chemokine and CD40L can induce non-hemolytic reaction after transfusion, transfusion-related acute lung injury (TRALI) and autoimmune disease during blood component storage. Pre-storage leucocyte deletion can prevent the release of leucocyte-derived chemokines, but not prevent the accumulation of platelet-derived chemokines. γ-irradiation or ultraviolet β irradiation is effective in preventing the increase of chemokines in the storage of platelet, thus prevents non-hemolytic febrile reaction after platelet transfusion. In this review, the recent advance in research of accumulation of chemokines and CD40L during blood component storage, and its effect on blood transfusion, as well as preventive measures are summarized.
Blood Platelets
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metabolism
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Blood Preservation
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Blood Transfusion
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CD40 Ligand
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blood
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Chemokines
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blood
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Humans
8.Expression of Mucosal Cyto-Chemokine mRNAs in Patients with Helicobacter pylori Infection.
Sill Moo PARK ; Jin Hee KIM ; Yo Han HONG ; Hye Ryung JUNG ; Joongwon PARK ; Jae Gyu KIM ; Bung Chul YOO
The Korean Journal of Internal Medicine 2001;16(4):230-235
BACKGROUND: Helicobacter pylori-induced destruction of the gastroduodenal mucosal barrier is initiated with mucosal infiltration of inflammatory cells. Cytokines and chemokines have been suggested to play important roles in the migration and activation of these inflammatory cells into the mucosa. The present study aimed to investigate expression rates of cyto-chemokine mRNAs using gastric mucosal biopsy specimens. METHODS: In 98 patients infected with Helicobacter pylori, mucosal mRNA expression rates of cytokines (IL-1beta, IL-6, and IL-10), C-C chemokines (macrophage inflammatory protein 1alpha [MIP-1alpha], and macrophage inflammatory protein 1beta [MIP-1beta], monocyte chemotactic and activating factor [MCAF], regulated on activation, normal T cell expressed and presumably secreted [RANTES]) and C-X-C chemokines (IL-8 and growth regulated alpha [GRO-alpha]) were examined using reverse transcription polymerase chain reaction (RT-PCR). RESULTS: The expression rates of mRNA for IL-8, GRO-alpha, MIP-1alpha and RANTES were significantly more increased in H. pylori-positive patients than in H. pylori- negative patients. However, the expressions of IL-1beta, IL-6 and IL-10 mRNA were statistically not different between two groups. After eradication of H. pylori, expressions of mRNA for three cytokines (IL-1beta, IL-6 and IL-10), four C-C chemokines (MIP-1alpha, MIP-1beta, MCAF and RANTES) and two C-X-C chemokines (IL-8 and GRO-alpha) were significantly decreased. CONCLUSION: These results suggest that C-X-C chemokines and some C-C chemokines play important roles in H. pylori-associated peptic ulcer diseases.
Adult
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Aged
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Aged, 80 and over
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Chemokines, CC/metabolism
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Chemokines, CXC/metabolism
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Chi-Square Distribution
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Cytokines/*metabolism
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Female
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Gastric Mucosa/*immunology/metabolism
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Helicobacter Infections/*immunology/metabolism
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*Helicobacter pylori
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Human
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Male
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Middle Age
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Prospective Studies
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RNA, Messenger/metabolism
9.Clinical Implications of Chemokines in Acute and Chronic Hepatitis C Virus Infection.
Yonsei Medical Journal 2011;52(6):871-878
Hepatitis C virus (HCV), a non-cytopathic positive-stranded RNA virus, is one of the most common causes of chronic liver diseases such as chronic hepatitis, liver cirrhosis and hepatocellular carcinoma. Upon HCV infection, the majority of patients fail to clear the virus and progress to chronic hepatitis C. Chemokines are small chemotactic cytokines that direct the recruitment of immune cells and coordinate immune responses upon viral infection. Chemokine production during acute HCV infection contributes to the recruitment of immune cells with antiviral effector functions and subsequent viral clearance. In chronic HCV infection, however, continuous production of chemokines due to persistent viral replication might result in incessant recruitment of inflammatory cells to the liver, giving rise to persistence of chronic inflammation and liver injury. In this review, we will summarize the roles of chemokines in acute and chronic settings of HCV infection and the clinical relevance of chemokines in the treatment of hepatitis C.
Antiviral Agents/therapeutic use
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Chemokines/*metabolism
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Hepatitis C/drug therapy/*immunology/*metabolism
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Hepatitis C, Chronic/drug therapy/*immunology/*metabolism
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Humans
10.Expression of adipokines in children with primary nephrotic syndrome and its association with hyperlipidemia.
Ru-Xin ZHANG ; Xuan ZHANG ; Bi-Li ZHANG ; Zhu-Feng LIU ; Shu-Xiang LIN
Chinese Journal of Contemporary Pediatrics 2021;23(8):828-834
OBJECTIVES:
To study the expression of adipokines in children with primary nephrotic syndrome (PNS) before and after treatment and its correlation with blood lipids, as well as the role of adipokines in PNS children with hyperlipidemia.
METHODS:
A total of 90 children who were diagnosed with incipient PNS or recurrence of PNS after corticosteroid withdrawal for more than 6 months were enrolled as subjects. Thirty children who underwent physical examination were enrolled as the control group. Venous blood samples were collected from the children in the control group and the children with PNS before corticosteroid therapy (active stage) and after urinary protein clearance following 4 weeks of corticosteroid therapy (remission stage). ELISA was used to measure the levels of adipokines. An automatic biochemical analyzer was used to measure blood lipid levels.
RESULTS:
Compared with the control group, the children with PNS had a significantly lower level of omentin-1 in both active and remission stages, and their level of omentin-1 in the active stage was significantly lower than that in the remission stage (
CONCLUSIONS
Omentin-1 may be associated with disease activity, dyslipidemia, and proteinuria in children with PNS. Blood lipid ratios may be more effective than traditional blood lipid parameters in monitoring early cardiovascular risk in children with PNS.
Adipokines
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Chemokines
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Child
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Cytokines/metabolism*
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GPI-Linked Proteins/metabolism*
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Humans
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Hyperlipidemias
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Lectins/metabolism*
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Lipids
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Nephrotic Syndrome/drug therapy*
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Proteinuria