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    08 February 2013, Volume 40 Issue 2 Previous Issue    Next Issue
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    Research progress of FLIP in cancer
    SHEN Jue, LI Yu-Feng, HE Zhen-Juan
    2013, 40 (2):  83-85. 
    Abstract ( 656 )   PDF (762KB) ( 1584 )   Save
    FLIP is a protein containing death domain. Human beings have three subtypes of c-FLIPL, c-FLIPS and c-FLIPR, which can inhibit the apoptosis of a variety of tumor cells. C-FLIPL plays a dual role in the apoptotic signal. The expression level of FLIP not only decides the opening and closing of the apoptosis pathway but also achieve the conversion of cells in the apoptotic signaling and proliferative signaling pathway. The regulation of FLIP’s expression is a multi-layered, involving multiple signaling pathways. FLIP will probably become an attractive death receptor signaling target of therapy.
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    Research progress of thioredoxin-related protein 14
    FU Zhi-Qin, XIE Xing, CHENG Xiao-Dong
    2013, 40 (2):  86-89. 
    Abstract ( 643 )   PDF (692KB) ( 1222 )   Save
    Thioredoxin-related protein 14 (TRP14), a new member of Trx family, is a novel disulfide reductase with conservative CPDC motif. Its structure and function are comparable to Trx, which is the representative member of Trx family. However, there are many differences. When tumor necrosis factor-α (TNF-α) induced cells to produce the active oxygen, TRP14 can as a sensor of the intracellular redox state, change oxidation state of dynein lifht chain (its substrate), thereby regulate NF-κB signaling pathways induced by TNF-α, MAPK and apoptosis signaling pathways.
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    Advances of GOLPH2 in tumors
    LI Wen-Zhi, WANG Xiang, CHEN Gang
    2013, 40 (2):  89-92. 
    Abstract ( 667 )   PDF (691KB) ( 1219 )   Save
    As a novel Golgi protein, GOLPH2 expression is associated with maintaining the structural integrity of the Golgi apparatus. As an oncoprotein, GOLPH2 expression is associated with malignant biological behavior of cancer cells. Important roles of GOLPH2 in the tumorigenesis and metastasis make it become a new target for tumor diagnosis and treatment.
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    Roles of apoptosis in the normal and tumor microenvironment
    DONG Shao-Ting, YANG Hong-Li, WANG Shuang
    2013, 40 (2):  92-95. 
    Abstract ( 705 )   PDF (690KB) ( 1609 )   Save
    Apoptosis is the autonomous death of cells, which is controlled by the genes and to maintain the homeostasis of the body. Apoptosis is the important mechanism in the cell’s growth and development. Recent studies have found that apoptosis can affect the neighboring cells physiological process in microenvironment through directly contact or release a series of regulatory factor, which plays an important roles in the construction of tumor microenvironment. Therefore, understanding the roles of apoptosis in the normal and tumor microenvironment has great significance for further study the pathogenesis, prevention and treatment of tumor.
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    Applications of induced pluripotent stem cell in cancer therapy
    ZHANG Zhi-Qing, ZHAO Qing-Hua
    2013, 40 (2):  96-99. 
    Abstract ( 641 )   PDF (689KB) ( 1972 )   Save
    Induced pluripotent stem cells (iPSCs) are derived from differentiated somatic cells through reprogramming in vitro. Similarly to embryonic stem cells (ESCs), iPSC have the ability of unlimited self-renewal and multiple differentiation potential. But they are without the constraints of immunology and ethics and acquire conveniently. Patient-specific iPSC provide an invaluable resource for disease modeling, drug discovery, regenerative therapy, immune therapy and cellular delivery vehicle in cancer therapy. Nowadays, the application of iPSC technology has made some progress in the treatment of tumors.
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    Tumor associated gene PFTK1
    ZHU Jun, YUE Wen-Tao
    2013, 40 (2):  100-102. 
    Abstract ( 744 )   PDF (680KB) ( 1511 )   Save
    PFTK1, an important member of cyclin dependent kinase Cdc2 family, is over expressed in many malignancies. PFTK1 involves in multiple processes, such as regulation of cell cycle, tumor invasion and metastasis, and the Wnt signal transduction pathway, which has a significant impact on prognosis of tumor.
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    Adoptive cellular immunotherapy for cancer
    SHANG Yi-Man, WANG Zi-Bing, MA Yi-Jie, ZHANG Yong, GAO Quan-Li
    2013, 40 (2):  103-106. 
    Abstract ( 839 )   PDF (692KB) ( 2373 )   Save
    Adoptive cellular immunotherapy (ACI) achieves the elimination and control of tumor by mobilizing the body's immune function. It also has targeted efficacy and mild untoward effects. Cytokine-induced killer cells and tumor-infiltrating lymphocytes have been widely used in clinic and have obtained preliminary efficacy. With the development and clinical application of the specific gene transfer of T cell, it will further increase the efficacy of immunotherapy. At present, improving cell culture technology and cell function and using with other treatment are the key links to improve the efficacy of ACI.
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    Assessment of CIK cells in adoptive cellular therapy
    WANG Wen-Hao, LI Gui-Xin, LIU Jin
    2013, 40 (2):  106-108. 
    Abstract ( 432 )   PDF (684KB) ( 1365 )   Save
    Cytokine-induced killer (CIK) cells therapy plays an important role in cancer adjuvant treatment. Researches show that the number of peripheral blood immunocytes will change if patients with cancer accept the treatment of CIK cells. The changes of T cell subsets, regulatory T cells are relatively obvious, which may be one of the standards that can evaluate the curative effect of CIK cells.
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    Transfer characteristics and therapeutic guide of level-Ⅰb lymph node in nasopharyngeal carcinoma
    HUANG Xiao-Guang, LIN Zhi-Xiong
    2013, 40 (2):  109-111. 
    Abstract ( 806 )   Save
    Because of the lymphatic drainage of the neck area level-Ⅰb of nasopharyngeal carcinoma is particular, and “skip” metastasis in the cervical lymph node is rare, the involved region of level-I b lymph node metastasis rate is low in nasopharyngeal carcinoma. In the three-dimensional radiotherapy era of precision radiotherapy,  there is no consensus on whether level-Ⅰb need to be prophylactic irradiated in the clinic.
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    MicroRNA and the biological behaviour of human breast cancer
    JIE Yong-Song, LI Lian-Hong
    2013, 40 (2):  111-114. 
    Abstract ( 769 )   PDF (690KB) ( 1450 )   Save
    MicroRNA (miRNA) controls the proliferation of breast cancer cells in many ways such as cell apotosis, cell cycle and methyltransferase. Also, it controls the metastasis of breast cancer cells in many ways such as microenvironment, epithelial-mesenchymal transition and vessel formation. Large amounts of recent studies indicate that miRNAs are specifically expressed in breast cancer tissue and play important roles in proliferation, metastasis and treatment of breast cancer.
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    Multiple molecular targets of resveratrol: anti-breast cancer mechanisms
    CHOU Feng-Qi, DING Xiao-Chao, MA Ping
    2013, 40 (2):  114-117. 
    Abstract ( 1032 )   Save
    Resveratrol, which is produced by natural plants, has various biological activities, including anti-inflammatory, antioxidant and anticancer properties. Recently, it is found that resveratrol can inhibit the proliferation and promote the apoptosis of breast cancer through multiple molecular targets, which provides a theoretical basis for resveratrol used in the treatment of breast cancer.
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    Changes of estrogen receptor, progesterone receptor and C-erbB-2 expressions in different scheme pre- and post-neoadjuvant chemotherapies for breast cancer
    SHI Peng-Liang, ZHANG Nai-Qian, ZHANG Guo-Qiang
    2013, 40 (2):  117-119. 
    Abstract ( 658 )   PDF (680KB) ( 1395 )   Save
    Neoadjuvant chemotherapy is widely used in the therapy of locally advanced breast cancer. In the recent studies, the expressions of ER, PR and C-erbB-2 in tumor may change in different scheme pre- and post-neoadjuvant chemotherapies for breast cancer. It is obviously changed in the neoadjuvant chemotherapy scheme of anthracyclines and paclitaxel/docetaxel, but hardly changed in anthracycline-based neoadjuvant chemotherapy scheme.
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    Lung adenocarcinoma progression schema
    YANG Zhen-Yu, FAN Zhi-Wen, ZHANG Lei
    2013, 40 (2):  120-122. 
    Abstract ( 867 )   PDF (676KB) ( 1882 )   Save
    Lung adenocarcinoma is usually thought to follow a linear multistep progression schema, that is precancerous lesions progress to adenocarcinoma in situ, and progress to micro-invasive adenocarcinoma, eventually some lung adenocarcinoma happen diffusion. However, recent ?ndings reveal that this linear progression schema might not occur in all lung adenocarcinoma subtypes, and some subtypes show a kind of non-linear progression schema. The study of these two kinds of schemas can help for early detection of lung adenocarcinoma.
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    Application of pemetrexed for the treatment of non-small-cell lung cancer
    LI Jun, XU Xiang-Ying
    2013, 40 (2):  123-126. 
    Abstract ( 801 )   PDF (692KB) ( 2744 )   Save
    Pemetrexed is a novel antifolate which is approved in the USA and Europe for the treatment of non-small-cell lung cancer (NSCLC). Researches reveal that pemetrexed enhances radiation-induced cell inactivation. A series of clinical trials of pemetrexed combined with radiotherapy for NSCLC also demonstrated that pemetrexed provides similar ef?cacy with lower toxicity and better tolerability than other third-generation chemotherapy drugs.
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    Gene polymorphisms in the nucleotide excision repair pathway and lung cancer susceptibility
    QIAN Ying-Ying, SHU Yong-Qian
    2013, 40 (2):  126-130. 
    Abstract ( 740 )   PDF (701KB) ( 1453 )   Save
    Nucleotide excision repair (NER) pathway is one of the principal ways of the repair of DNA damage. The single nucleotide polymorphisms (SNP) of its key genes such as xeroderma pigmentosum group A (XPA) gene, excision repair cross complementing1 (ERCC1) gene and xeroderma pigmentosum group D (XPD) gene may be associated with differences in the DNA repair capacity and may influence an individual’s risk of lung cancer, because the variant genotype in those polymorphisms might destroy or alter repair function.
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    Surgical treatment of esophagogastric junction adenocarcinoma
    SHI Gui-Dong, FU Mao-Yong
    2013, 40 (2):  130-133. 
    Abstract ( 890 )   PDF (691KB) ( 1552 )   Save
    There are a variety of surgical treatments of advanced esophagogastric junction cancer, type Ⅰ、Ⅱ mainly by transthoracic approach, part of the type Ⅱ by transabdominal approach, type Ⅲ mainly by left thoracoabdominal approach (LTA) or transabdominal. Intraoperative lymph node dissection is one of the most important factors which affect the postoperative survival rate. The cardia right lymph node (NO.1), the cardia left lymph node (NO.2), gastric lesser curvature (NO.3) and left gastric artery side (NO.7) should do regular cleaning.
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    Detection of the tumor markers in patients with gastric precancerous lesions
    LIU Zhong-Juan, CHENG Xin-Qi, GUO Zi-Jian, ZHAO Li-Na, QIU Ling
    2013, 40 (2):  134-137. 
    Abstract ( 767 )   PDF (691KB) ( 1506 )   Save
    It is confirmed that chronic atrophic gastritis (CAG) which is caused by Helicobacter pylori is the main cause of gastric precancerous lesions. CAG is also the key determinant in gastric cancer risk assessment, which affects pepsinogen and gastrin-17 secretion. Most of the gastric cancer patients with poor prognosis, and non-invasive tools for gastric cancer screening and diagnosis are lacking. Therefore, the early detection of gastric cancer in order to reduce the disease mortality is necessary. Pepsinogen and gastrin-17 are biomarkers of gastric mucosa and gastric antra. The serological testing for the stomach-specific biomarkers offers the possibility to know preneoplastic gastric mucosal conditions.
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    Application of PET-CT in liver cancer
    SUN Li, LI Gong, ZHAO Ying, XU Cen-Cen
    2013, 40 (2):  137-140. 
    Abstract ( 708 )   PDF (749KB) ( 1326 )   Save
    Positron emission tomography-computed tomography (PET-CT) plays an important role in the diagnosis and treatment of liver cancer.18F-FDG PET-CT imaging-positive rate is low due to a variety of factors affecting the hepatoma cells. But the joint imaging can significantly improve the diagnostic positive rate and provide the basic information for treatment selection and prognosis.PET-CT is better than conventional imaging techniques in the diagnosis and therapy monitoring for metastatic liver cancer.
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    Preoperative neoadjuvant therapy for locally advanced rectal cancer
    MEI Lan, XU Xiang-Ying
    2013, 40 (2):  141-144. 
    Abstract ( 685 )   PDF (693KB) ( 1430 )   Save
    Preoperative radiotherapy combined with chemotherapy and (or) targeted therapy not only reduces the local recurrence of locally advanced rectal cancer and increases the rate of anal preservation and pathologic complete response, but also improves patient compliance. Preoperative neoadjuvant therapy will gradually become the standard treatment for locally advanced rectal cancer.
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    Diagnosis, treatment and prognosis of uterine cervical neoplasms complicated with pregnancy
    QIANG Su-Feng, HUANG Yong
    2013, 40 (2):  145-148. 
    Abstract ( 638 )   PDF (688KB) ( 1155 )   Save
    The incidence of cervical neoplasms complicated with pregnancy is rising, with delaying of reproductive age. Because of the prevalence of cytology in pregnancy, cervical neoplasms complicated with pregnancy are mostly detected early. All patients with cytological abnormalities should undergo colposcopy, and when necessary, they should undergo cervical biopsy. Conization is reserved for patients with suspected invasion. In cases of invasive carcinoma detected up to the 12th week of pregnancy, immediate treatment is prioritized. Regarding diagnoses made during the second trimester, in early-stage invasive cancers, delay of therapy seems to be safe, fetal pulmonary maturity can be awaited. And the use of neoadjuvant chemotherapy to stabilize the disease until the time of delivery appears to be viable. Doctors should draw up personalized program for the patients with cervical neoplasms complicated with pregnancy according to stage of disease, gestational weeks and the patient’s desire for continued pregnancy. Cervical neoplasms complicated with pregnancy are mostly early-stage invasive cancers, so prognosis is good.
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    Inhibitory effect of antisense miR-30a-5p on glioma cell growth in vivo
    SUN Ji-Kui, JIA Zhi-Fan, PU Pei-Yu, WANG Guang-Xiu, ZHANG An-Ling, YANG Wei-Dong
    2013, 40 (2):  149-152. 
    Abstract ( 697 )   PDF (1848KB) ( 1423 )   Save
    Objective To study the inhibitory effect of knocking down miR-30a-5p on the U87 human glioma xenograft growth and its possible mechanism. Methods Nude mice bearing subcutaneous U87 human glioblastoma were established and treated with miR-30a-5p antisense oligonucleotides (AS-miR-30a-5p) subcutaneous injection. Tumor size was measured every other day until the observation period ended. Researchers executed the animals after the treatment, stripped tumor tissues and extracted RNA and protein. Real-time PCR were conducted to detect the expression of miR-30a-5p. The histopathological characteristics and proliferation and apoptosis biological characters (including SEPT7, PCNA, cyclinD1, MMP-2, apoptosis related factor P53, bcl-2 and caspase3)were evaluated by HE and immunohistochemical staining, Western blot analysis respectively, and the cell apoptosis was detected by TUNEL method. Results In AS-miR-30a-5p treated group, the tumor growth was delayed and the final tumor volume was smaller than that in the control and scr-ODN treated group (F=7.167, P<0.05), and the expression of miR-30a-5p was knocked down. The expression of PCNA、cyclinD1 were significantly down-regulated while P53、SEPT7 and caspase3 up-regulated. Apoptotic index was increased significantly. Conclusion As-miR-30a-5p suppresses the growth of U87 human gliomas xenografts significantly. Malignant phenotype of tumors are reversed to a considerable degree. Therefore, miR-30a-5p can be a candidate for targeted therapy of human glioma.
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    Survey of quality of life for patients with breast ductal carcinoma in situ and analysis of related factors
    JIANG Bei-Qi, FU Yun, WU Yi, CHENG Xiao-Lin, LI Zheng-Dong, ZHUANG Zhi-Gang
    2013, 40 (2):  153-156. 
    Abstract ( 662 )   PDF (693KB) ( 1570 )   Save
    Objective To study the quality of life (QOL) of patientswith ductal carcinoma in situ (DCIS) and to analyze the relevant factors affecting their QOL. Methods A total of 84 patients with DCIS and 125 patients with invasive breast cancer were surveyed. Researchers used SF-36 to assess the QOL of participants at one year after operation. Some information of patients were analyzed the relationship to SF-36 score, such as age, the type of surgery, endocrine therapy, education, marital status, working status and health insurance. Results Compared to normal women, patients with DCIS had lower QOL in physical function (P=0.029), bodily pain (P=0.039), general health (P=0.033) and mental health (P=0.003). Patients with invasive breast cancer also had poorer QOL in physical function (P=0.002), bodily pain (P=0.002), vitality (P=0.002), general health (P=0.002) and mental health (P=0.001). QOL of DCIS patients were similar to that of invasive breast cancer patients, except that score of physical function (P=0.032) and vitality (P=0.040) were better in DCIS patients. Endocrine therapy significantly affected the score of QOL of DCIS patients. DCIS patients with endocrine therapy had poorer score in physical function (P=0.034), bodily pain (P=0.046), general health (P=0.031), vitality (P=0.042) and mental health (P=0.002). Conclusion Patients with DCIS have poor QOL at one year after operation. Endocrine therapy significantly reduces their QOL.
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