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Table of Content

    06 August 2012, Volume 39 Issue 7 Previous IssueNext Issue
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    Tumor multidrug resistance and apoptosis evasion
    SUN Fei, QING Chen
    2012, 39 (7): 483-485.
    Abstract( 774) PDF(710KB) ( 2096) Save
    Most anticancer drugs inhibit tumor cell growth by inducing apoptosis. Apoptosis-evasion, also enhancement of antiapoptosis ability (e.g. anti-apoptosis related genes over-expression or pro-apoptotic related genes loss, etc.) may lead to tumor cell multidrug resistance. Many researches show that apoptosis-evasion is one of the important factors resulting in tumor multidrug resistance.
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    Negative effects of protein tyrosine phosphatase SHP-1 in cell signaling
    PENG Gang, CAO Ru-Bo, WU Gang
    2012, 39 (7): 485-488.
    Abstract( 816) PDF(649KB) ( 1670) Save
    SHP-1 is the protein tyrosine phosphatase which is mainly expressed in the cytoplasm of hematopoieticderived cells, and it is the key factor to change the levels of intracellular phosphorylation. SHP-1 can generate different intracellular signals in different cells, and it can play various functions.
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    Pregnane X receptor and tumor multidrug resistance
    QIAO En-qi, TANG Jin-Hai, WU Jian-Zhong
    2012, 39 (7): 489-492.
    Abstract( 795) PDF(646KB) ( 1734) Save
    The overexpression of P-glycoprotein (P-gp) and its coding gene mdr1 is regarded as the classic mechanism of multidrug resistance (MDR). Recent studies find that pregnane X receptor (PXR) can mediate the expression of P-gp. It is confirmed that PXR can also inhibit apoptosis of tumor cells. Therefore, preventing the activation of PXR specifically may be a new method to prevent MDR.
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    Mechanism of tumor angiogenesis
    GENG Liang, HUA Bao-Jin
    2012, 39 (7): 492-497.
    Abstract( 810) PDF(665KB) ( 2425) Save
    Based on the theory of tumor angiogenesis, the vascular system is necessary for the advance and metastasis of the tumor. To inhibit or even cure the tumor, the researchers all over the world have made a great many of studies on the mechanism of tumor angiogenesis and have acquired some achievements. Based on the findings, a lot of factors are involved in tumor angiogenesis, and they constitute the complex regulating network through interaction at the molecular and cellular level.
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    Effect of adiponectin in malignant tumor neovascularization
    MA Ruo-Bing, PAN Yue-Long, WANG Jian
    2012, 39 (7): 497-500.
    Abstract( 805) PDF(643KB) ( 1703) Save
    Adiponectin is recently described as an adipocyte secreting cytokine, which is abundant in human plasma. Adiponectin plays important roles not only in glucose and lipid metabolism but also in the development and progression of several obesityrelated malignancies. Vascular formation is a key step in the cancer growth and metastasis. Current reserches find that the effect of adiponectin in cancer vascular growth still has great differences. This review discusses the effect of adiponectin in malignant tumor neovascularization, and reveals that adiponectin can be a new vasoinhibitor.
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    Quantitative evaluation of tumor angiogenesis using ultrasound molecular imaging
    QIAN Xiao-Qin, WANG Wen-Ping
    2012, 39 (7): 500-503.
    Abstract( 811) PDF(641KB) ( 1452) Save
    This paper summarizes the new progress of the research of the targeted microbubble ultrasound contrast agents and ultrasound molecular imaging in tumor angiogenesis. There are two constructing methods of targeted microbubble ultrasound contrast agents. Targeted new blood vessels microbubble unltrasound contrast agents are mainly divided into the connection of alpha (V) beta3 antibody, αVβ3 integration antibody and connecting VEGFR2. The quantitative analysis of targeted microbubble adhering to tumor target and the evaluation of the correlation between targeted microbubble adhering to tumor neovascular endothelial cell and tumor local pathological microvessel density suggest that ultrasound molecular imaging can be noninvasive, quick, repeated, dynamic and quantitative evaluate tumor angiogenesis and indirectly reflect the malignant tumor tissue proliferation activity and its biological characteristics.
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    Reactive oxygen species and tumor therapy
    ZHANG Hou-Li, CUI Shu-Xiang
    2012, 39 (7): 504-507.
    Abstract( 945) PDF(643KB) ( 3055) Save
    Oxidative stress can achieve the purpose of tumor therapy by accelerating the death of tumor cells. As a major molecule generated from the body's oxidative stress reaction, reactive oxygen species (ROS) exerts the antitumor efforts by promoting apoptosis, necrosis and autophagy. The drugs which could increase the level of ROS in cells have received more and more people's attention, and this provide a new research direction for the clinical treatment of tumors.
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    Resveratrol and cancer metastasis
    CHEN Hai-Xia, YANG Yao-Qin
    2012, 39 (7): 508-509.
    Abstract( 784) PDF(622KB) ( 1510) Save
    Resveratrol is a natural phytoalexins. In vivo and vitro experiments show that resveratrol could inhibit tumor metastasis by multiple approaches, such as influencing the expression level of matrix metalloproteinases and inhibitors, inhibiting tumor angiogenesis and interferencing signaling pathways, et al.
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    Cancer cachexia diagnosis and therapy
    LIU Zi-Feng, LI Gui-Xin
    2012, 39 (7): 510-513.
    Abstract( 834) PDF(660KB) ( 1898) Save
    Cancer cachexia (CC) caused by cancer is a syndrome with complicated symptoms. Traditional therapies usually give interventions for more nutrition intake at CC late stage and take weight as the outcome marker. Lots of clinical trials demonstrate that the effect is not satisfactory. Recent studies show that the level of NF-κB decreased, termination of the breakdown of myofibrillar proteins, the serum proteins and lean body mass increased and function improvement after targeting proteasome at early stage of CC combined with traditional therapy.
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    Microglia in brain metastasis tumor
    LI Yan, BAI Ying
    2012, 39 (7): 513-515.
    Abstract( 652) PDF(633KB) ( 1451) Save
    Microglia (MG) is recognized as the main immune effector in central nervous system injury and disease. MG can regulate the tumorigenesis and development of brain metastases tumor (BMT) by different ways. Studing the roles and mechanisms of MG in BMT will provide new insights into the prevention and treatment of BMT.
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    Cadherins and triple-negative breast cancer
    SHI Xue-Bing, WANG Lu
    2012, 39 (7): 516-518.
    Abstract( 678) PDF(634KB) ( 1525) Save
    Cadherins that mediate the adhesion of the same type of cells by specific binding to calciumdependent adhesions of the same type with cadherins mainly consist of three subtypes including E-cadherin, P-cadherin and N-cadherin. In recent years, more and more studies have indicated that cadherins are closely related to triple-negative breast cancer (TNBC) and play an important role in prognosis and treatment of TNBC.
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    Targeted therapy for triplenegative breast cancer
    LI Rong-Hui, DU Cai-Wen, ZHANG Guo-Jun
    2012, 39 (7): 519-522.
    Abstract( 750) PDF(650KB) ( 1973) Save
    Triplenegative breast cancer (TNBC) is a special subtype of breast cancer which is invalid to endocrine therapy. AntiHer2 targeted therapies such as herceptin and lapatinib are not suitable to TNBC. At present, conventional chemotherapy is the only way for the medical therapy of TNBC. Thus, searching for novel therapeutic agents for TNBC is one of hot researches of breast cancer. New targeted therapy drugs such as PARP1 inhibitors, EGFR inhibitors, CXCR4 inhibitors, antiangiogenesis drugs, Src tyrosine kinase inhibitor, and mTOR inhibitor are being researched.
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    Detection technique of circulating tumour cells in lung cancer
    XIA Fan, ZHAO Teng, WANG Yan
    2012, 39 (7): 523-525.
    Abstract( 851) PDF(626KB) ( 1925) Save
    Circulating tumor cells (CTCs) are essential for establishing recurrence and metastasis in malignant tumors. Detecting CTCs can help for early detection of the cancer metastases and recurrences, and also can help for evaluating prognostic and guiding treatment. CTCs detection technique mainly include screening and separation technology which contains immune magnetic separation technology and reverse transcriptasepolymerase chain reaction and so on. With the development of technique, there is a new technique named ctcchip contains both screening and separation functions.
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    Individual comprehensive therapy study for esophageal carcinoma
    YIN Jun, LI Tao
    2012, 39 (7): 526-529.
    Abstract( 649) PDF(644KB) ( 1517) Save
    Recently, with the development of the medical technique includes surgery, radiotherapy, chemotherapy and molecular targeted therapy, multi-subject combined modality therapy for esophageal carcinoma has been become a tendency instead of surgery alone. Any single treatment is hard to improve the curative effect of treatment for esophageal carcinoma. Systemic individual comprehensive therapy for the different patients with esophageal carcinoma is likely to reduce recurrence rate, improve survival rates as well as to improve the quality of life.
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    Regulatory relationships between microRNAs and DNA methylation in gastric cancer
    GU Yong-Juan, ZHAO Qiu, GUO Ren-Hua
    2012, 39 (7): 529-532.
    Abstract( 730) PDF(647KB) ( 1434) Save
    MicroRNAs (miRNAs) are a class of small (22 nucleotides) noncoding RNAs which play important roles in diverse biological and pathological processes. The dysregulation of miRNA expression is closely related to the development and progression of malignant tumors in humans. DNA methylation is a kind of epigenetic modification in human genome. Both hypermethylation and hypomethylation of DNA are closely related to different kinds of tumors, including gastric cancer.
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    Gastric cancer chemotherapy related genes
    QIN Yong, GUO Hong
    2012, 39 (7): 533-537.
    Abstract( 706) PDF(659KB) ( 1895) Save
    The expression of genes have an important effect to gastric cancer chemotherapy. Some genes are related the therapeutic efficacy of drugs, some genes are related the untoward effects of drug, and some genes are related the sensitivity of the tumor to drug. Chemotherapy related genes may play an important guiding role to improve the curative effect of chemotherapy patients. In recent years, the gastric cancer chemotherapy related genes have made great progress, especially in platinum, fluorouracil, paclitaxel and targeted medicine related genes.
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    Small interfering RNA in gastrointestinal cancer
    JU Feng, ZUO Jun-Bo, XIA Jia-Zeng
    2012, 39 (7): 538-540.
    Abstract( 652) PDF(634KB) ( 1431) Save
    SiRNA comes from doublestranded RNA, which is processed into a small molecular fragment by Dicer. 2125nt siRNA, as the key effector molecules to the RNAi process, can inhibit gene expression with high specificity and high efficiency in mammalian cells. Currently, RNAi has been widely applied in a variety of cancer. RNAi has many active research explorations of the tumor development, metastasis and treatment in gastrointestinal cancer.
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    Role of Numb in tumors
    WANG Chao, ZHANG Chu-Yao, FENG Wei-Wei
    2012, 39 (7): 541-544.
    Abstract( 723) PDF(643KB) ( 1864) Save
    Numb, one of the important cell fate determinants, plays a key role in regulation of nerve system development, and it is closely related to the occurrence of tumors. It is proven that Numb is implicated in the processes of occurrence, invasion and metastasis of tumors through regulating the way of cell division, cell polarity, epithelialmesenchymal transitions and several signal pathways, e.g., Notch, Hh, p53. The expression levels of Numb in cells are related to the malignant degree and prognosis of tumors. It is vital to explore the role of Numb in tumors for treating tumors at the standpoint of Numb.
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    Notch signal pathway and the pathogenesis of multiple myeloma
    LIU Qin-Qin, GUO Dong-Mei, TENG Qing-Liang
    2012, 39 (7): 544-546.
    Abstract( 768) PDF(670KB) ( 1376) Save
    Notch signal pathway can regulate the morphogenesis, apoptosis and cellular proliferation of normal tissues and organs, which plays an important role in regulating hematopoietic cells proliferation and differentiation in bone marrow microenvironment. The occurrence and development of multiple myeloma (MM) are closely related to the bone marrow microenvironment in which many signal pathways are involved. Recent studies show that Notch signal pathway promotes the development and progression of many cancers including MM, which plays key roles in tumor invasion and drug resistance. This review focus on the recent findings on Notch signal pathway in MM, and reveals that Notch signal pathway will be identified as a potential new therapeutic target in MM.
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    Correlation between the levels of serum squamous carcinoma antigen and the prognosis of cervical squamous carcinoma
    JING Jie-Xian, WU Xiao-Hong, DU Li-Li, TIAN Bao-Guo, HAN Cun-Zhi, ZHAO Xian-Wen
    2012, 39 (7): 547-551.
    Abstract( 814) PDF(659KB) ( 2035) Save
    Objective To analyze the correlation between the levels of squamous cell carcinoma antigen (SCCAg) and the clinicopathological characteristics of patients with cervical squamous carcinoma. To study the relationship of serum SCCAg levels of patients with recurrent cervical squamous carcinoma and disease prognosis and to investigate the survival rate of patients with recurrent cervical squamous carcinoma. Method ELISA method was used to determine the serum SCCAg levels for the patients, which included 300 cases before treatment and 500 cases after treatment. Results (1) Single factor analysis indicated that, before the treatment, the serum SCCAg levels were closely related to clinical stages, lymphatic metastasis, and deep myometrial invasion (t=3.01, P<0.05; t=6.81, P<0.001; t=3.01, P<0.05; respectively). However, they were not related to patient′s age, vascular embolization and tumor growth type (t=0.77, t=1.12, t=1.06; respectively, all P>0.05). Multifactor logistic regression analysis showed that the pretreatment SCCAg levels of patients were related to clinical stages, cavum pelvis lymphatic metastasis and myometrial invasion (χ2=2.88, P=0.0084; χ2=2.612, P=0.0156; χ2=2.570, P=0.0171; respectively). (2) Overall, recurrent disease developed in 180 of the 500 patients with cervical squamous carcinoma. One hundred and sixtyone recurrent patients showed elevated SCCAg levels (161/180, 89.4%). For the 60 patients who showed elevated SCCAg levels without any clinical symptoms as well as no sign of tumors by iconography, the median time for signs of elevating levels of serum SCCAg was 2.3 months. The longest time range was 150d between the increasing levels of the tumor markers and the appearance of the imaging features of pachygyria while the patients condition was going on. The 160 patients out of the 180 cases with recurrent cervical squamous carcinoma who were followed up had a median survival time of 9 months, with an average of 20 months. The total 3 year survival rate and 5 year survival rate was respectively 23.4% and 17.8%. (3) Single factor analysis indicated that recurrent patients' clinical stages, recurrent region and recurrent post treatment SCCAg levels were closely related with patients′ survival time (χ2=10.26, P<0.005; χ2=14.65, P<0.005; χ2=8.97, P<0.01; respectively). There was no statistical difference between the survival rate of recurrent patients with increased SCCAg level and patients without increased SCCAg levels (χ2=0.89, P>0.05). Multiple factor analysis indicated that the clinical stages, recurrent post treatment SCCAg levels of patients with recurrence were independent prognostic factors (χ2=10.3372, P=0.0013; χ2=4.3889, P=0.0362; respectively). Conclusion The pretreatment SCCAg levels are closely related to patients' clinical stages, cavum pelvis lymphatic metastasis and deep myometrial invasion. Serum SCCAg levels are important for the advanced detection of cervical squamous carcinoma recurrence and prognosis prediction.
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    Effects of oldhamianoside Ⅱ on the invasive ability of prostatic carcinoma cells
    WANG Yan, WANG Feng-Ling, MOU Yan-Ling, LI Jun
    2012, 39 (7): 551-554.
    Abstract( 688) PDF(904KB) ( 1580) Save
    ObjectiveTo observe the effects of oldhamianoside Ⅱ on the invasive ability of prostatic carcinoma DU-145 cells, and to investigate the potential mechanism. MethodsAfter treatment of DU-145 cells with oldhamianoside Ⅱ, MTT assay was used to test the effect of oldhamianoside Ⅱ on the cell proliferation.The invasive ability was assessed with a transwell cell culture chamber. Immunocytochemistry stain was used to investigate the expression of matrix metalloproteinase (MMP-2) and CXCchemokine receptor 4 (CXCR4). ResultsThe proliferation of DU-145 cells was inhibited after treatment with oldhamianoside Ⅱ. In vitro invasion assay indicated that the cells moved through the membrane were (180.3±14.6)/field in the control group, while decreased to (100.4±1.5), (80.2±2.7) and (60.1±5.3)/field in 0.25, 0.5 and 1 μg/mL oldhamianoside Ⅱ treated DU145 cells respectively. Comparing to control group, the cells of oldhamianoside Ⅱ groups moved through the membrane were decreased remarkably (P<0.05). Immunocytochemistry showed that the expression of MMP-2 and CXCR4 were decreased of oldhamianoside Ⅱ groups. ConclusionsOldhamianoside Ⅱ can inhibit the invasiveness of DU-145 cells, which is related to the down regulation the expression of MMP-2 in DU-145 cells. Oldhamianoside Ⅱ can inhibit the prostate cancer cells metastasis to the bone, which is related to the down regulation the expression of CXCR4 in DU-145 cells.
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