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期刊信息
  • 临床肿瘤学杂志
    主管:解放军无锡联勤保障中心
    主办:解放军东部战区总医院
    编辑出版:临床肿瘤学杂志编辑部
    主编:秦叔逵
    编辑部主任:龚新雷
    地址:南京市杨公井34标34号
    邮编:210002
    电话:(025)84400143;80864363
    E-mail: lczlx@vip.163.com
    邮发代号:28-267
    刊期:月刊
    定价:每期15元,全年180元
    标准刊号: ISSN 1009-0460
    CN 32-1577/R
     
Table of Content
31 August 2016, Volume 21 Issue 8
论著
Inhibitory effects of recombinant fusion protein TAT-OSBP-MKK6(E)on the proliferation and metastasis of cisplatin-resistant human epithelial ovarian cancer
YIN Shuqin, KANG Jiali, YUAN Jin, YANG Ying, SHUAI Rong
Chinese Clinical Oncology. 2016, 21 (8):  673. 
Abstract ( 427 )   PDF(pc) (1881KB) ( 292 )   Save
Objective To investigate the effect of recombinant fusion protein TAT-OSBP-MKK6(E)on the proliferation,invasion and metastasis of cisplatin(DDP)-resistant human epithelial ovarian cancer cell SKOV3/DDP. Methods MTT assay was used to analyze the influence of TAT-OSBP-MKK6(E)alone or in combination with a autophagy inhibitor 3-methyladenine(3-MA) on the sensitivity of DDP in SKOV3/DDP cells.The autophagy level was observed by monodansylcadaverin staining. The mRNA and protein expression levels of Beclin 1 were evaluated by QPCR and Western blotting after challenge with fusion protein. The abilities of invasion and migration were evaluated by Transwell assay. Results The half-inhibition concentration(IC50)of SKOV3/DDP cells was(37.62±2.63)μg/ml. After being exposure to 10,20 and 40 μg/ml fusion protein,the IC50 of SKOV3/DDP cells was decreased to(17.07± 0.88),(11.08 ±0.57)and(1.96±0.31)μg/ml,respectively(P<0.001). The inhibition of autophagy by 3-MA abolished the sensitivity of SKOV3/DDP cells to DDP induced by TAT-OSBP-MKK6(E). The autophagy fluorescence of SKOV3/DDP in the group of TATOSBPMKK6(E) and TATOSBPMKK6(E)plus 3-MA were 824±107 and 459±128,higher than 306±143 of control group(P<0.05). The mRNA and protein expression levels of Beclin 1 elevated with the increase of TAT-OSBP-MKK6(E) concentration(10, 20, 40 μg/ml),and the differences between each concentration group and control group were statistically significant(P<0.01). The expression of Beclin 1 protein in SKOV3/DDP cells was also different among control group, TATOSBPMKK6(E)group and DDP plus TAT-OSBP-MKK6(E)group(P<0.05). The expression of Belin1 protein were the highest in the TAT-OSBP-MKK6(E)plus DDP group(0.876±0023) followed by that of TAT-OSBP-MKK6(E)group(0.564±0.021). Cell migration and invasion assay showed that TAT-OSBPMKK6(E)could inhibit the invasion and migration ability of SKOV3/DDP cells,and the difference of TAT-OSBP-MKK6(E)plus DDP group and TAT-OSBP-MKK6(E) group were significant compared with control group(P<0.05). No significance was observed between DDP group and control group(P>0.05). Conclusion Recombinant fusion protein TAT-OSBP-MKK6(E)can effectively inhibit the proliferation,invasion and migration of SKOV3/DDP cells,probably by inducing autophagy and up-regulating Beclin 1 expression.
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Effects of different cisplatin chemotherapy patterns on vasculogenic mimicry of ovarian cancer cell SKOV3 and the possible mechanisms
WU Xiaohua,CHEN Lin,SUN Yanan
Chinese Clinical Oncology. 2016, 21 (8):  680. 
Abstract ( 413 )   PDF(pc) (2936KB) ( 367 )   Save
Objective To explore the effects of low-dose metronomic chemotherapy(LDM)and maximum tolerated-dose chemotherapy(MTD)on vasculogenic mimicry(VM)of ovarian epithelial cancer cell SKOV3 and the possible mechanisms. Methods The primary tumor cells were obtained through injecting cisplatin by different chemotherapy schedules(LDM,MTD and control group without chemotherapy)in the nude mice bearing SKOV3 ovarian cancer xenografts. Three groups of primary cells were cultured in threedimensional cell culture model to compare the VM formation ability. The proliferative and invasive ability of each group was evaluated by MTT and Transwell chamber test in vitro respectively. The expression level of CD133 and aldehyde dehydrogenase1(ALDH1)in the primary cells were analyzed by Western blotting and VM formation differences of CD133+ALDH1+cells and CD133-ALDH1-cells were observed by fluorescence-activated cell sorting(FACS). Results The tumor inhibition rates of MTD group and LDM group were 25.87% and 51.52%. Primary tumor cells formed VM in MTD group in only about 6 hours, while in control group and LDM group were 9 hours and 12 hours respectively. After 48 h,the vasculogenic mimicry density(VMD)of MTD group,control group and LDM group was 29.60±9.55,18.70±4.97 and 11.20±2.60,with statistical significance(P<0.05). Compared to LDM group and control group,the cell proliferation of MTD group was significantly higher from the third day(P<0.05). Transwell chamber test showed that the cells of LDM group got through the maxtrix film was 87.33±19.58,much less than 156.93±22.77 of MTD group and 112.13±16.59 of control group(P<0.05). Western blotting suggested that the levels of CD133 and ALDH1 proteins in primary tumor cells of MTD group were 0.402±0.034 and 0.418±0.020,in control group were 0.338±0.046 and 0.325±0.011,in LDM group were 0.296±0.042 and 0.318±0.012. The differences among the 3 groups had statistic significance(P<0.05). When CD133+ALDH1+cells and CD133-ALDH1-cells were cultured with the same density of 5×104/ml,the former formed VM within 6 h,while the latter did not form any after 48 h. Little VM was observed after 24 h when CD133-ALDH1-cells were cultured with the density of 1×105/ml. Conclusion The tumor cells with partial tumor stem cell properties to be enriched easier in MTD than in LDM probably. These cells could influence the tumor blood supply and result in bad prognosis.
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Inhibitory effect of bafilomycin A1 on proliferation and autophagy of touge squamous cell carcinoma Tca8113 cells
ZENG Wen, PAN Yiyun, LI Shiqin, ZHANG Rui, FEI Jimin
Chinese Clinical Oncology. 2016, 21 (8):  687. 
Abstract ( 405 )   PDF(pc) (1203KB) ( 259 )   Save
Objective To explore the inhibitory effect of bafilomycin A1(Baf-A1)on cell proliferation and autophagy of touge squamous cell carcinoma Tca8113 cells. Methods Tca8113 cells were cultured with Baf-A1(0.1,0.5 μmol/L), and cells without treatment were set as control group. The cell proliferation was determined at 0,24,48 and 72 h by MTT assay in control group and Baf-A1 group. Flow cytometry was applied to measure cell cycle treated with 0.5 μmol/L Baf-A1 for 72 h. Western blotting and immunofluorescence were used to analyze autophagy marker LC3B protein expression. Autophagosome formation was observed by transmission electron microscope. Results Baf-A1 could dose-dependently inhibit the proliferation of Tca8113 cells. The highest proliferative inhibition was observed at 72 h after cells treated with 0.5 μmol/L BafA1. Compared with control group, Tca8113 cells in Baf-A1 group increased in sub-G1 and G1 phase(P<0.05), and decreased in S and G2/M phase(P<0.05). LC3B-II expression of Baf-A1 group was 1.83±0.23,which was significantly higher than 0.79±0.18 of control group(P<0.05). Immunofluorescence showed that little LC3B could be seen in control group, while large amount of LC3B puncta was observed in Baf-A1 group after 72 h. Compared with control group,large amount of autophagosomes were observed and the formation of autolysosomes increased in Baf-A1 group. Conclusion Baf-A1 has a toxic effect on the proliferation of Tca8113 cells. It may be related to cell cycle arrest and autophagy inhibition.
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Expression and clinical significance of SMG 1, mTOR and Raptor in breast cancer tissues
ZHAO Qian,DILIXIATI Jinsihan,TULUHONG Shalier
Chinese Clinical Oncology. 2016, 21 (8):  692. 
Abstract ( 423 )   PDF(pc) (1392KB) ( 286 )   Save
Objective To investigate the expression of suppressor with morphogenetic effect on genitalia-1(SMG 1),mammalian target of rapamycin(mTOR)and regulatoryassociated protein of mTOR(Raptor)in breast cancer and analyze their clinical significance. Methods From January 2014 to July 2015,samples of 68 breast cancer tissues,40 adjacent normal breast tissues,and 40 breast fibroadenoma tissues were collected. The expression of SMG 1 in the above tissues was detected by immunohistochemistry SP method. Real-time quantitative PCR(QPCR)was applied for the detection of mTOR and Raptor levels. Correlation of SMG 1,mTOR and Raptor with clinicopathological features of breast cancer was studied. Spearman correlation analysis was used to analyze the correlation between SMG 1 expression and mTOR, Raptor expression. Results The positive expression rate of SMG 1 in breast cancer tissues was 27.9%(19/68),lower than 77.5%(31/40) of adjacent normal breast tissues and 82.5%(33/40)of breast fibroadenoma tissues(P<0.05). The levels of mTOR and Raptor in breast cancer were 2.754±0.213 and 4.137±0.626,higher than those of adjacent normal breast tissues and breast fibroadenoma tissues(P<0.05). SMG 1 expression was related to tumor size,lymph node metastasis and histological grade(P<0.05). mTOR was related to tumor size, TNM stage and histological grade(P<0.05). Raptor expression was related to tumor size,lymph node metastasis and histological grade (P<005). SMG 1 expression was negatively correlated with mTOR and Raptor expression(r=-0.547,r=-0.415,P<0.05),and mTOR expression was positively correlated with Raptor expression (r=0.664,P<0.05). Conclusion There are high expression of mTOR and Raptor, and low expression of SMG 1 in breast cancer tissues. Expression of mTOR,Raptor and SMG 1 are correlated with tumor size and histological grade,indicating that SMG 1, mTOR and Raptor may play an important role in the occurence and development of breast cancer.
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Expression and clinical significance of RASA1 in non-small cell lung cancer
HUANG Yan, YANG Jiyuan
Chinese Clinical Oncology. 2016, 21 (8):  698. 
Abstract ( 400 )   PDF(pc) (1283KB) ( 274 )   Save
Objective To investigate the expression of Ras p21 protein activator 1(RASA1)in non-small cell lung cancer(NSCLC)and the correlation with clinicopathological characteristics. Methods From Mar 2013 to Jan 2016, 202 cases of NSCLC tissues and 60 cases of adjacent normal tissues were collected. The expression of RASA1 in those above tissues was detected by immunohistochemical SP method and tissue microarray technique. The relationship between clinicopathological characteristics and the expression of RASA1 was analyzed. Results The high expression rate of RASA1 in NSCLC tissues was 74.8%(151/202),lower than 93.3%(56/60)of adjacent normal tissues with statistical significance(P=0.002). The expression of RASA1 in NSCLC tissues was correlated with pathological types(P=0.000),but not with gender,age,lymphnode metastasis and clinical stage(P>0.05). Conclusion RASA1 was low expressed in NSCLC tissues,which may play a role in the occurrence and development of NSCLC as a potential tumor suppressor.
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Analysis of the relationship between polymorphism of PI3K/Akt gene and efficacy of platinumbased chemotherapy for gastric cancer
LIN Xiuxin, DENG Wenjing, YU Gengsheng, LV Huazhu, LI Chunming
Chinese Clinical Oncology. 2016, 21 (8):  702. 
Abstract ( 403 )   PDF(pc) (857KB) ( 307 )   Save
Objective To investigate the relationship of single nucleotide polymorphisms(SNPs)of phosphatase and tensin homolog deleted on chromosome ten(PTEN)and phosphatidylinositol 3-kinase catalytic alpha polypeptide(PIK3CA)of PI3K/Akt pathway with efficacy of platinum-based chemotherapy in patients with advanced gastric cancer. Methods Four tag SNPs of PTEN genes(rs532678,rs926091,rs11202609 and rs17431184)and 3 tag SNPs of PIK3CA genes(rs2459693,rs3729679 and rs12494623)from Beijing Han population database published by International HapMap Project(Hap Map)were screened using Haploview software.The peripheral blood samples of 158 patients from Jan 2012 to Dec 2015 with advanced gastric cancer were collected and MassArray mass spectrometry array was used to determine genotype. The short-term efficacy of platinum-based chemotherapy was evaluated by RECIST 1.1 creteria after two cycles of chemotherapy. Then the patients were assigned into sensitive group (CR+PR) and insensitive group(SD+PD). The relationship between sensitivity and above SNPs genotype/allele was analyzed. Results In 158 patients with advanced gastric cancer,the genotypes and the allele distribution of 7 SNPs in PTEN and PIK3CA genes were in line with the Hardy-Weinberg equilibrium. There were 83 patients in sensitive group(3 cases of CR and 80 cases of PR)and 75 patients in insensitive group(42 cases of SD and 33 cases of PD)after 2 cycles' chemotherapy. PIK3CA rs3729679 and rs12494623 SNPs were associated with the sensitivity of platinum-based chemotherapy in patients with advanced gastric cancer. Patients harboring mutation genes(rs3729679 G, rs12494623 T) had rather low sensitivity and an increased risk of insensitivity with the statistical significant differences(P<0.05). The remaining PIK3CA SNPs and PTEN SNPs loci were unrelated with sensitive rates and risk of insensitity(P>0.05). Conclusion PIK3CA rs3729679 and rs12494623 SNPs were associated with the sensitivity of platinumbased chemotherapy in patients with advanced gastric cancer. Patients harboring rs3729679 G or rs12494623 T are not sensitive to chemotherapy and have a higher risk for being insensitive to chemotherapy. It is helpful to predict the efficacy of platinum-based chemotherapy in patients with advanced gastric cancer.
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Department of Gastroenterology,the Affiliated Jiangning Hospital of Nanjing Medical University,Nanjing 211100,China
MIAO Yingying,QIU Wei, WANG Jianning, ZHU Zuming, ZHAI Qizhi
Chinese Clinical Oncology. 2016, 21 (8):  708. 
Abstract ( 420 )   PDF(pc) (1542KB) ( 239 )   Save
Objective To investigate the correlation of vascular endothelial growth factor C(VEGF-C),and vascular endothelial growth factor receptor 3(VEGFR-3)with the infection of helicobacter pylori(Hp)and clinicopathological characteristics in gastric carcinoma. Methods The infection with Hp in 40 patients with gastric carcinoma was detected by 13C breath test and improved Giemsa. The expression of VEGF-C,VEGFR-3 in 40 cases of gastric carcinoma and their adjacent tissues were detected by immunohistochemical SP method. Results The infection of Hp in 40 gastric carcinoma patients was 65.0%. The expressions of VEGF-C,VEGFR-3 in gastric carcinoma tissues were(8.74±0.84)×10-2 and(3.64±1.96)×10-2,and in adjacent tissues they were(1.23±0.38)×10-2 and(0.90±0.18)×10-2. The expressions of VEGF-C,VEGFR-3 in gastric carcinoma were significantly higher than those of adjacent tissues(P<0.05). There was a positive correlation between VEGF-C and VEGFR-3(r=0.51,P<0.05). The expressions of VEGF-C,VEGFR-3 were related to the depth of invasion,differentiation,lymph node metastasis and TNM stage(P<0.05), but not with tumor size(P>0.05). The expression of VEGF-C,VEGFR-3 in Hp-positive gastric carcinoma tissues were(11.72±3.07)×10-2 and(8.71±2.15)×10-2,which were higher than (8.48±1.11)×10-2and(5.37±1.05)×10-2 in Hp-negative gastric carcinoma tissues,with significant differences(P<0.05). Conclusion Infection of Hp and the expressions of VEGF-C,VEGFR-3 are associated with the ooccurrence and progression of gastric carcinoma. The infection of Hp may be correlated with lymphangiogenesis.
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Expression of transcription factor POU5F1 in colorectal cancer tissues and its significance
WANG Deyuan, NIE Limin
Chinese Clinical Oncology. 2016, 21 (8):  712. 
Abstract ( 366 )   PDF(pc) (1450KB) ( 414 )   Save
Objective To investigate the expression of transcription factor POU5F1 in colorectal cancer tissues and its relationship with clinicopathological features and prognosis. Methods One hundred and forty-two cases of paraffin-embedded colorectal cancer tissues and 86 cases of paraffin-embedded adjacent mucosa tissues were collected from January 2011 to July 2013. The expression of POU5F1 was measured by immunohistochemical SP method in 142 cases of colorectal cancer and 86 cases of adjacent mucosa tissues. The relationship of POU5F1 expression with clinicopathological parameters was analyzed. According to follow-up data,the prognosis of patients with different expression level of POU5F1 was investigated. The factors influencing prognosis was analyzed by Cox proportional hazard model. Results The positive expression of POU5F1 was localized in the nucleus and cytoplasm. The high expression rate of POU5F1 in colorectal cancer tissues was 47.2%(67/142),higher than 23.3%(20/86)of adjacent normal mucosa tissues,and the difference was statistically significant(P<0.05). The expression of POU5F1 was not related to sex,age,tumor location,distant metastasis,CEA,CA50 and CA199 of colorectal cancer,but it was related to the depth of invasion,lymph node metastasis,TNM stage and differentiation(P<0.05). The median overall survival(OS) was 26.4 months in patients with high expression,worse than 33.6 months in patients with low expression(P<0.05). Cox proportional hazard model analysis showed that the depth of invasion,lymph node metastasis,distant metastasis,TNM staging and POU5F1 expression were independent factors influencing OS. Conclusion The expression of POU5F1 in colorectal cancer tissues is associated with the degree of invasion,lymph node metastasis,TNM stage,differentiation and OS,and it has certain value in the diagnosis and prognostic prediction of colorectal cancer.
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Expression and clinical significance of FOXC2 and E-cad in colon cancer tissues
WANG Jingmiao, JIA Xihua, WANG Xiaobo, AI Xiaoqing, SONG Taining
Chinese Clinical Oncology. 2016, 21 (8):  718. 
Abstract ( 372 )   PDF(pc) (1114KB) ( 251 )   Save
Objective To investigate the expression and clinical significance of forkhead C2(FOXC2)and E-cadherin(E-cad)in colon cancer tissues. Methods From Jan 2014 to Mar 2016,70 cases of colon cancer and 30 adjacent normal tissues were collected. Immunohistochemical SP method was used to determine the expression of FOXC2 and E-cad in those tissues. The correlation of the two proteins in colon cancer tissues,and the relationship of the two proteins with pathological features were analyzed. Results The expression of FOXC2(74.3%,52/70) in colon cancer tissues was significantly higher than that in adjacent normal tissues(20.0%,6/30)with statistic significance(P<0.001). The expression of E-cad(21.4%,15/70)in colon cancer tissues was lower than that in adjacent normal tissues(80.0%,24/30)with statistic significance(P<0.001). The expression of FOXC2 and E-cad was related with TNM staging of tumor,depth of invasion and lymph node metastasis(P<0.05),and no association was observed in age,gender,tumor size and histological grading(P>0.05). The two proteins were negatively correlated in colon cancer tissues(r=-0.728,P<0.05). Conclusion FOXC2 shows high expression in colon cancer tissues, while Ecad is low expressed. Meanwhile,a negative correlation is observed between the two proteins,suggesting that FOXC2 and E-cad may be involved in the occurrence and development of colon cancer.
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Expression and diagnostic value of serum miRNA-21 and miRNA-203 in epithelial ovarian cancer
ZENG Yu,CHEN Chen,WU Wei,YAO Hui,GAO Lingjuan
Chinese Clinical Oncology. 2016, 21 (8):  722. 
Abstract ( 374 )   PDF(pc) (870KB) ( 280 )   Save

Objective To investigate the expression of microRNA 21(miR-21)and microRNA203(miR-203)in epithelial ovarian cancer(EOC), and the diagnostic value of them in combination with serum carbohydrate antigen 125(CA125)in EOC. Methods Serum miR-21 and miR-203 expression in 40 cases of patients with EOC(EOC group),40 cases of epithelial ovarian benign tumor patients(benign group)and 42 healthy women(control group)were detected by QPCR; Serum CA125 concentration was tested by electrochemiluminescence immunoassay;The correlation between miR-21, miR-203 and the clinicopathological features in EOC patients was analyzed. The receiver operating characteristic curve(ROC)was used to evaluate sensitivity and specificity of miR-21, miR-203 and CA125 alone or in combination. Results The expressions of serum miR-21 and miR-203 in EOC group were 2.27±0.48 and 3.61±0.71,higher than 1.20±0.22 and 1.47±0.38 in benign group,as well as 1.00±0.33 and 1.00±0.28 in control group with significant difference(P<0.05). There was no significant difference between benign group and control group(P>0.05). miR-21 and miR203 expression were correlated with clinical stages and lymph node metastasis(P<0.05),but not with age,menopause status,pathological types and CA125 levels(P>0.05). The diagnostic specificity of CA125 alone was 82.50%,and diagnostic sensitivity of CA125,miR-21 and miR-203 combined detection was 95.00%. They were the highest among those of single or combined detection.
Conclusion miR-21 and miR-203 may play an oncogene role in the development of EOC. The combined detection of serum CA125,miR-21 and miR203 are expected to be used in screening for EOC due to improving the diagnostic sensitivity.

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Clinical study of raltitrexed plus nedaplatin combined with concurrent helical tomotherapy for locally advanced nasopharyngeal carcinoma
DING Wei,JIANG Wanron,SUN Xiangdong,ZHOU Bin,FU Chenchun, ZHANG Xinliang
Chinese Clinical Oncology. 2016, 21 (8):  727. 
Abstract ( 384 )   PDF(pc) (839KB) ( 421 )   Save
Objective To investigate the efficacy and toxicities for patients with locally advanced nasopharyngeal carcinoma(NPC)treated by helical tomotherapy(HT)in combination with raltitrexed plus nedaplatin chemotherapy(RN+HT)or with docetaxel plus nedaplatin chemotherapy(DN+HT). Methods A total of 84 diagnosed local/regional advanced NPC patients from Mar 2011 to Apr 2015 were enrolled in this study,among whom 31 cases received RN+HT treatment(raltitrexed 2.5 mg/m2 iv,d1;nedaplatin in total 75 mg/m2 iv,d1-d5),and 53 cases received DN+HT treatment(docetaxel 35-40 mg/m2 iv,d1,d8;nedaplatin in total 75 mg/m2 iv,d1-d5). All the patients were treated with chemotherapy for 2 cycles with 21 days as a cycle. Long-term efficacy and toxicities were compared between the two groups. Results The median follow-up period was 21.5 months of 84 patients. There were 1 case of local recurrence, 2 cases of distant metastasis,and 2 cases of death in RN+HT group. And in DN+HT group,there were 2 case of local recurrence,3 cases of distant metastasis and 3 cases of death. The 2-year survival rate of RN+HT and DN+HT groups was 93.5%and 94.3%(P>0.05),and the 2-year progressionfree survival rate was 90.3%and 90.6%(P>0.05). The most common acute adverse reactions were 1-2 grade mucosa reaction,skin injury,hematologic toxicities,weight loss,parotid injury,sphagitis and nausea/vomitting. Nausea/vomitting was higher in DN+HT group than in RN+HT group(P<0.05),and no differences were found in other adverse actions between the two groups(P>0.05). Chronic injuries included skin injury, subcutaneous fibrosis and xerostomia,and no differences were found between the two groups(P>0.05). Conclusion RN+HT is effective and well-tollerated for locally advanced NPC.
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临床应用
Clinical efficacy of docetaxel plus cisplatin sequentially combined with S-1 as adjuvant chemotherapy for gastric cancer after operation
AN Yuji,SHENG Lijun,SONG Pengyuan,ZHANG Zhen,PANG Min,HE Weina,ZHANG Weihua
Chinese Clinical Oncology. 2016, 21 (8):  732. 
Abstract ( 375 )   PDF(pc) (855KB) ( 233 )   Save
Objective To evaluate the clinical efficacy and safety of docetaxel plus cisplatin sequentially combined S-1 for patients with gastric cancer of ⅢB-ⅢC stage after operation. Methods A total of 32 patients with gastric cancer of ⅢB-ⅢC stage treated with adjuvant chemotherapy 4 weeks after D2 radical resection were analyzed retrospectively. The adjuvant chemotherapy regimen was as follows:docetaxel 75mg/m2 iv d1;cisplatin 25mg/m2 iv d1-d3. Six cycles were applied with 21 days as a cycle. Then S-1 was orally given as follows:80 mg/m2 for 2 times daily from d1-d14 and 21 days were a cycle. S-1 was applied to 1 year after operation. Patients' 3-year survival,3-year recurrence-free survival and adverse reactions were observed. Results All the patients accomplished chemotherapy in plan. The 1-,2-and 3-year survival rate of 32 patients was 90.6%,81.2% and 65.0%,respectively. The 1-,2-and 3-year recurrence-free survival rate was 90.6%,81.2% and 50.4%,respectively. The clinical efficacy was not associated with pathological stage,but with number of lymph nodes(P<0.05). Patients bearing metastatic lymph nodes three or less had better 3-year survival rate compared with those bearing lymph node more than 3(78.6% vs. 54.2%, P<0.05). Adverse reactions included bone marrow suppression,gastrointestinal symptoms and hair loss,mainly in grade 1-2. Conclusion Docetaxel plus cisplatin sequentially combined with S-1 as adjuvant chemotherapy for gastric patients with high risk can bring better overall survival, recurrence-free survival,and adverse effect are well-tolerated.
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综述与讲座
The function of long noncoding RNAs in breast cancer carcinogenesis, development and its potential clinical significance
ZHAO Hanting,LIN Chaoyi,XU Yingchun,WANG Hongxia
Chinese Clinical Oncology. 2016, 21 (8):  736. 
Abstract ( 608 )   PDF(pc) (931KB) ( 378 )   Save
Long noncoding RNAs(lncRNAs)refer to noncoding RNA molecules with the length between 200-100 000 nucleotides. They were considered as transcriptional‘noise’without biological function. However,recent studies show that lncRNAs have a wide participation in gene silencing,transcriptional activation,cell cycle and differentiation,chromosome configuration modification,and many other biological functions,making lncRNAs a new hot spot in the field of cancer research. In this review,we give a systematic description of the relationship between lncRNAs and breast cancer carcinogenesis,progression,molecular subtyping,treatment resistance,epithelialmesenchymal transition and exosomes. We hope that this review will help to promote a better understanding of the sophisticated molecular regulation mechanisms of lncRNAs in breast cancer development and pioneer new ideas for diagnostic methods and specific therapeutic targets for breast cancer.
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Research on metastasis associated gene 2 mediating invasion and metastasis of tumor
WANG Chao,ZHOU Chenfei,ZHANG Jun
Chinese Clinical Oncology. 2016, 21 (8):  744. 
Abstract ( 381 )   PDF(pc) (842KB) ( 468 )   Save
Metastasis associated gene 2(MTA2)is a member of metastasis-associated gene family. Protein alignment homology of human MTA proteins and coding sequence of functional domain revealed high homology of MTA2 with MTA1. MTA2 is one of the components of nucleosome remodeling deacetylase(NuRD)complex which have chromatin remodeling and histone deacetylating properties. It can also interact with some transcription factors and involve into gene transcriptional regulation. MTA2 is overexpressed in various kinds of malignancies and closely associated with tumor invasion and metastasis,which indicates that MTA2 may play vital role in tumor metastasis. Herein,we will review the expression,biological function and the molecular mechanism of MTA2 in tumor invasion and metastasis.
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Advances of epigenetic alterations in colorectal cancer
WEI Yan, LI Kainan, BI Jingwang
Chinese Clinical Oncology. 2016, 21 (8):  748. 
Abstract ( 399 )   PDF(pc) (876KB) ( 270 )   Save
The fundamental processes of driving the initiation and progression of colorectal cancer(CRC)is the accumulation of a variety of genetic changes,but its regulation mechanism has not been fully explained. Over the past decades,major advances have been made in our understanding of cancer epigenetics,particularly regarding microRNA(miRNA),aberrant DNA methylation and alterations in histone modification states. Assessment of CRC has revealed that virtually all CRCs have altered miRNA expression and aberrantly methylated genes. As with gene mutations in the cancer genome, these epigenetic alterations have a functional role in CRC. The epigenetic alterations in CRC have developed as clinical biomarkers for diagnostic,prognostic and therapeutic applications. Progress in this area suggests that these epigenetic alterations will be commonly used in the near future to direct the prevention and treatment of CRC.
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Progress of long non-coding RNA in esophageal carcinoma
FAN Yanxin, SHI Weihong, TANG Weiwei, CAO Xiufeng
Chinese Clinical Oncology. 2016, 21 (8):  753. 
Abstract ( 400 )   PDF(pc) (931KB) ( 250 )   Save
With the innovations sequencing technologies,biotechnology and computational biology,long noncoding RNAs(lncRNAs)are being identified and characterized at a rapid pace. Recent findings reveal that lncRNAs are implicated a series of cancer development. These lncRNAs interact with DNA,RNA,protein molecules and/or their combinations,acting as an essential regulator in chromatin organization,and transcriptional and post-transcriptional regulation. Their abnormal expression confers the cancer cell activities for tumor initiation, growth and metastasis. This review here will emphasize their aberrant expression and function in cancer,and the roles in cancer diagnosis and therapy will also be discussed. LncRNAs have emerged as an essential regulator in almost all aspects of biology. Accumulating evidence suggests that lncRNAs play an important role in tumorigenesis. In this review,we will briefly review the structure and function of lncRNAs, and then emphasize their aberrant expression and their functional roles in esophageal carcinoma,diagnosis and therapy.
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Progress of video endosopic inguinal lymphadenectomy in vulvar cancer
LIU Chai‘’e, LU Yan
Chinese Clinical Oncology. 2016, 21 (8):  760. 
Abstract ( 375 )   PDF(pc) (831KB) ( 391 )   Save
The presence of lymph node metastasis is the most important prognostic factor for vulvar cancer. Although inguinofemoral lymphadenectomy has demonstrated good oncological efficacy,it is plagued with high morbidity such as groin breakdown and infection. This surgical method causes long-time low quality of life and delay of postoperative chemotherapy and radiotherapy. Gynecologic oncologists have introduced video endoscopic inguinal lymphadenectomy(VEIL)for the management of vulvar cancer. This method can avoid the groin long incision effectively, reduce postoperative morbidity, shorten recovery time and hospital stay, and improve prognosis.
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