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    25 February 2021, Volume 13 Issue 1 Previous Issue    Next Issue
    Research progress in clinical application of tumor stem cells
    LI Chong, XU Binghe
    2021, 13 (1):  1-6.  doi: 10.3969/j.issn.1674-5671.2021.01.01
    Abstract ( 612 )   PDF (1676KB) ( 1079 )   Save
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     esearch progress in multiomics of hepatocellular carcinoma
    MO Qiuyn, GONG Wenfeng, YU Hongping, TANG Weizhong
    2021, 13 (1):  7-13.  doi: 10.3969/j.issn.1674-5671.2021.01.02
    Abstract ( 699 )   PDF (1420KB) ( 714 )   Save
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    Global outlook for primary liver cancer: prevalence,risk factors,and population attribution scores
    ZHOU Zewen, LIU Yingchun, XIANG Bangde, YU Hongping
    2021, 13 (1):  14-21.  doi: 10.3969/j.issn.1674-5671.2021.01.03
    Abstract ( 880 )   PDF (1445KB) ( 2146 )   Save
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     CircRNA and gastrointestinal neoplasms: progression and opportunity
    ZHANG Mingxin, LU Ning, WU Kaichun
    2021, 13 (1):  22-27.  doi: 10.3969/j.issn.1674-5671.2021.01.04
    Abstract ( 4771 )   PDF (1190KB) ( 812 )   Save
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    Inhibitory effect of CASC19 on colorectal cancer through maintaining macrophage M1 polarization
    GE Jiang, WU Jing, ZHANG Shutian, MIN Li, LIU Kuiliang, LI Qian, LI Nanshan
    2021, 13 (1):  28-33.  doi: 10.3969/j.issn.1674-5671.2021.01.05
    Abstract ( 2403 )   PDF (11207KB) ( 59 )   Save
    Objective To investigate the role of long non-coding RNA CASC19(the cancer susceptibility 19) in maintaining the polarized state of M1 macrophage and its effect on the growth of colorectal cancer cells. Methods Mononuclear lymphoma Thp1 cells were induced to degenerate into unpolarized macrophage M0, which were further induced to polarize into the classical activated M1 macrophage and the alternative activated M2 macrophage. The expressions of the M1 and M2 macrophage molecular markers and the CASC19 were detected by RT-qPCR, and the polarized state of macrophages and transfection efficiency of CASC19 were confirmed. The colorectal cancer cells SW480 were stimulated by the supernatant of M1 macrophage(M1 SI-MC group) and Negative control supernatant(M1 NC-MC group) that knocked down CASC19. Real-time dynamic imaging and MTS staining were used to assess the cell proliferation ability, and Transwell assays was used to measure the cell migration ability. Results RT-qPCR showed that polarized macrophages were successfully induced. The expression level of CASC19 in M1 macrophage was higher than that in M0 and M2 macrophage(P<0.05). Compared with the M1 NC-CM group, the supernatant of M1 macrophage with knocking down CASC19 had weaker inhibition on the proliferation and migration of colorectal cancer cells SW48(P<0.001). After knocking down CASC19 in M1 macrophage, the expression levels of M1 molecular markers CD40 and IL-1β were decreased, while the expression levels of M2 molecular markers CD206, IL-10 and CD163 were increased(P<0.05). Conclusion CASC19 knockdown can weaken the inhibition of proliferation and migration of M1 macrophage on colorectal cancer cells, which may be achieved by eliminating the maintenance effect of CASC19 on the polarized state of M1 macrophage.
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    Matrine-inhibiting radiation resistance in esophageal squamous cell carcinoma by inducing miR-433-3p expression
    LIU Ying, FENG Dabing, WANG Jizhao, ZHANG Cheng, ZHANG Lu, ZHANG Mingxin, CHEN Nanzheng
    2021, 13 (1):  34-39.  doi: 10.3969/j.issn.1674-5671.2021.01.06
    Abstract ( 2104 )   PDF (14749KB) ( 112 )   Save
     Objective To investigate the effect of Matrine on radiation resistance and miR-433-3p expression in esophageal squamous cell carcinoma. Methods To construct the overexpression of miR-433-3p and RAD21 and knock down the radiation resistance of Eca-109R cells. The Eca-109 and Eca-109R cells before and after transfection were treated with different radiation doses(0 Gy, 2 Gy, 4 Gy, 6 Gy and 8 Gy) and different concentrations(0.5 mg/mL, 1.0 mg/mL, 2.0 mg/mL, 3.0 mg/mL, 4.0 mg/mL and 5.0 mg/mL) of Matrine;  the expression of miR-433-3p and RAD21 were detected by qRT-PCR and western blot, and the cell viability was detected by CCK-8 assay. Dual luciferase reporter gene assay was used to evaluate the interaction between miR-433-3p and RAD21 in Eca-109 cells. Results Different concentrations of Matrine inhibited the cell viability of radiation resistant Eca-109R cells and reestablished the radiosensitivity(P<0.05). The miR-433-3p was lowly expressed in Eca-109R cells(P<0.05), the knockdown of miR-433-3p enhanced the cell viability of Eca-109R cells, while the Matrine could relieve the promotion of miR-433-3p knockdown on Eca-109R cell viability effect(F=5.213, P<0.05). RAD21 was highly expressed in Eca-109R cells(P<0.05). Overexpression of RAD21 could enhance the cell viability of Eca-109R cells and reverse the inhibitory effect of miR-433-3p on Eca-109R cell activity(F=4.554, P<0.05). Dual luciferase reporter gene assay indicated that miR-433-3p specifically interacted with the 3′UTR region of RAD21. Conclusion Matrine can inhibit the expression of RAD21 by inducing the high expression of miR-433-3p and reestablish the radiosensitivity of esophageal squamous cell carcinoma.
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    TRPM7 affects the proliferation and epithelial-mesenchymal transition of brain glioma cell through PI3K/AKT/ERK signaling pathway
    WU Pengfei, WANG Yun, QIN Hu, LIU Yang, WU Jinze, WANG Zengliang
    2021, 13 (1):  39-44. 
    Abstract ( 241 )   PDF (10533KB) ( 57 )   Save
    Objective  To investigate the effect of silent melastatin transient receptor potential channel 7(TRPM7) on the proliferation and epithelial-mesenchymal transition of brain glioma cells and the underlying mechanism. Methods The TRPM7 expression in human normal astrocyte cell line HA1800 and glioma cell lines(U251, U87 and U373) were detected by qRT-PCR and Western blot. U251 cells were divided into the U251 group(untransfected U251 cells), U251/shNC group and U251/shTRPM7 group, then the expression of TRPM7 was detected by qRT-PCR and Western blot;  the cell proliferation ability was detected by cell clone formation assay;  the cell migration and invasion ability were detected by Transwell migration and invasion experiments;  the expression of E-cadherin and Vimentin was detected by cellular immunofluorescence assay;  the expression of PI3K/AKT/ERK signaling pathway-related proteins were detected by Western blot. Results Compared with HA1800 cells, TRPM7 was highly expressed in glioma cell lines(P<0.05). Silencing TRPM7 reduced the expression of TRPM7 in U251 cells(P<0.001), and the ability of cell proliferation, migration and invasion were significantly reduced(P<0.01);  E-cadherin expression was increased(P<0.001) and Vimentin expression was decreased(P<0.01);  the expression level of PI3K protein was down-regulated(P<0.01), and the phosphorylation level of AKT protein and ERK1/2 protein were also significantly reduced(P<0.01). Conclusion Silencing TRPM7 can inhibit the proliferation, migration, invasion ability and epithelial-mesenchymal transformation of U251 cells, which may be related to the PI3K/AKT/ERK signaling pathway.
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    Effect of miR-106b on radiosensitivity of hepatoma cells and its mechanism
    WANG Zheng, CHEN Chuang, DING Zhilong, XU Zhen, LYU Chunyang
    2021, 13 (1):  45-50.  doi: 10.3969/j.issn.1674-5671.2021.01.08
    Abstract ( 275 )   PDF (12072KB) ( 39 )   Save
    Objective To investigate the effect of miR-106b on the radiosensitivity of hepatoma cells and its possible mechanism. Methods The expression of miR-106b in human hepatoma cell lines HepG2, SMMC-7721, SK-HEP-1, Huh7 and normal hepatocyte QSG7701 were detected by qRT-PCR. The HepG2 cells were transfected with miR-106b siRNA(miR-106b down-regulated group), and the blank control group and negative control group were set up. After irradiated by different doses(0 Gy, 2 Gy, 4 Gy, 6 Gy, 8 Gy), cell plating efficiency(PE) and cell survival fraction(SF) were determined by cell clone formation assay. After irradiated by 6 Gy, the proliferation and apoptosis of cells in each group were detected by CCK-8 method and flow cytometry; the protein expressions of p-PI3K/PI3K, p-AKT/AKT, PCNA and Bax were detected by Western blot. Results Compared with QSG7701 cells, the expression level of miR-106b in HepG2, SMMC-7721, SK-HEP-1, and Huh7 cells was increased(all P<0.05), and the expression level of miR-106b in HepG2 cells was the highest. The results of clone formation experiment showed that PE and SF levels in HepG2 cells were reduced with the increase of irradiation dose (all P<0.05) after irradiated by different doses(0 Gy, 2 Gy, 4 Gy, 6 Gy, 8 Gy), and there was no statistical significance in PE and SF levels between 6 Gy and 8 Gy irradiation (both P>0.05). After 6 Gy irradiation , compared with the blank control group and the negative control group, the proliferation ability of HepG2 cells and the protein expression levels of p-PI3K/PI3K, p-AKT/AKT and PCNA in miR-106b down-regulated group were decreased(all P<0.05), while the apoptosis rate and the protein expression level of Bax were increased(all P<0.05). Conclusion The down-regulation of the expression of miR-106b can inhibit the proliferation and induce the apoptosis of HepG2 cells, while enhance the radiosensitivity, and the underlying mechanism may be related to the blocking of PI3K/AKT pathway activation.
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    Effects of miR-130a on angiogenesis in exosomes of esophageal squamous cell carcinoma cells and its mechanism
    ZHENG Senyuan, LIU Fang, HE Xiaolei, ZHANG Zhiqiang
    2021, 13 (1):  50-55.  doi: 10.3969/j.issn.1674-5671.2021.01.09
    Abstract ( 282 )   PDF (16450KB) ( 32 )   Save
    Objective To investigate the effect of miR-130a in esophageal squamous cell carcinoma exosomes on angiogenesis and its mechanism. Methods The exosomes secreted by esophageal epithelial cells HEEC, esophageal squamous cell carcinoma cells TE-13 and Eca-109, and transfected miR-130a mimic, miR-130a inhibitor and its negative control(NC) exosomes of Eca-109 cells were extracted, and co-incubated with human umbilical vein endothelial cells HUVEC. The proliferation, migration and tubule formation abilities of HUVEC cells in each group were detected by MTT, Transwell chamber and tubule formation experiments;  the expression level of miR-130a was detected by qRT-PCR;  the phosphorylation levels of PI3K and AKT as well as the expression levels of PTEN, Ang1 and iNOS were detected by Western blot. Results After HUVEC cells were co-incubated with TE-13 and Eca-109 cell exosomes, the proliferation, migration and tubule formation abilities were enhanced(P<0.01);  and the phosphorylation levels of PI3K and AKT and the expression levels of Ang1 and iNOS were up-regulated(P<0.001), while the expression level of PTEN was down-regulated(P<0.001). The qRT-PCR results showed that the expression level of miR-130a in TE-13 and Eca-109 cell exosomes were higher than that in HEEC exosomes(P<0.01). The down-regulation of miR-130a expression in Eca-109 cell exosomes could inhibit the proliferation, migration and tubule formation abilities of HUVEC cells(P<0.01), while down-regulated the phosphorylation of PI3K and AKT and the expression levels of Ang1 and iNOS (P<0.001), and up-regulated the expression level of PTEN(P<0.001). Conclusion The miR-130a in the exosomes of esophageal squamous cell carcinoma exosomes may induce tumor angiogenesis by activating the PTEN/PI3K/AKT signaling pathway of vascular endothelial cells.
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     miR-491-59 regulates the proliferation and migration of hepatoblastoma cells by targeting FGFR4
    ZHAO Tianjiao, GENG Jianlei, WEN Chan, REN Hui, LIU Feng, WEI Ping
    2021, 13 (1):  56-61.  doi: 10.3969/j.issn.1674-5671.2021.01.10
    Abstract ( 309 )   PDF (9923KB) ( 61 )   Save
    Objective To investigate the effect of miR-491-5p targeting and regulating FGFR4 on the proliferation and migration of hepatoblastoma and its possible mechanism. Methods The expressions of miR-491-5p and FGFR4 mRNA in 15 cases of pediatric hepatoblastoma tissues and adjacent normal tissues, the normal hepatocytes cells LO2 and hepatoblastoma cells HuH-6 were detected by qRT-PCR, and the expression level of FGFR4 protein was detected by Western blot. TargetScan database predicted the target of miR-491-5p, and the relationship between miR-491-5 and FGFR4 was detected by luciferase activity assay. After the mimic NC, miR-491-5p mimic, pcDNA3.1 plasmid and pcDNA3.1-FGFR4 plasmid were all transfected into HuH-6 cells, the expression of FGFR4 was detected by qRT-PCR and Western blot, the cells proliferation was detected by CCK-8, the cell migration assay was detected by Transwell assay, and the expression of GSK3β/β-catenin signaling pathway related proteins was detected by Western blot. Results The expression level of miR-491-5p in pediatric hepatoblastoma tissues and HuH-6 cells was lower than that in adjacent normal tissues and hepatocyte cells LO2(P<0.05), while the expression level of FGFR4 was higher than that in adjacent normal tissues and hepatocyte cells LO2(P<0.05). TargetScan database predicted that miR-491-5p and FGFR4 had binding sites. Compared with the mimic NC group, overexpression of miR-491-5p inhibited the expression of FGFR4, the proliferation and migration of hepatoblastoma cells HuH-6, and the ratios of p-GSK3β/GSK3β, p-β-catenin/β-catenin and p-C-myc/C-myc(all P<0.05). Compared with mimic+Pc group, overexpression of FGFR4 could reverse the inhibitory effect of miR-491-5p on the proliferation and migration of HuH-6 cells, and the ratio of p-GSK3β/GSK3β, p-β-catenin/β-catenin and p-C-myc/C-myc(all P<0.05). Conclusion miR-491-5p negatively regulates FGFR4 to inhibit the proliferation and migra-tion of hepatoblastoma cells, which may be related to the inactivation of GSK3β/β-catenin signaling pathway.
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     Expression of histone deacetylase 2 in hepatocellular carcinoma and its clinical significance
    CHEN Zhong, LIN Liyan, CHENG Bianqiao, LIN Renhe, JIANG Xiaoling
    2021, 13 (1):  62-66.  doi: 10.3969/j.issn.1674-5671.2021.01.11
    Abstract ( 409 )   PDF (5111KB) ( 259 )   Save
    Objective To investigate the expression of histone deacetylase 2(HDAC2) in hepatocellular carcinoma(HCC) tissues and its relationship with prognosis. Methods The expression of HDAC2 protein in hepatocellular carcinoma and corresponding adjacent normal tissues were detected by the Western blot and immunohistochemical methods, and the relationship between the expression level of HDAC2 and clinicopathological parameters and prognosis was analyzed. Results The expression of HDAC2 protein in HCC tissues was significantly higher than that in normal tissues(P=0.025), and its expression level was correlated with tumor differentiation, vascular invasion and relapse (all P<0.05). Multivariable Cox analysis showed that the high expression of HDAC2 was an independent risk factor for overall survival of patients with hepatocellular carcinoma(HR=12.255, 95%CI:2.865-52.411, P=0.001). Conclusion HDAC2 is highly expressed in HCC tissues, and patients with high expression of HDAC2 have poor prognosis, implying that it can be a molecular marker for prognosis of HCC.
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    The expression of sirtuin 4 in gastric cancer and its prognostic value
    MEI Jia, LI Jun
    2021, 13 (1):  67-71.  doi: 10.3969/j.issn.1674-5671.2021.01.12
    Abstract ( 289 )   PDF (4049KB) ( 185 )   Save
    Objective To investigate the expression of sirtuin 4(SIRT4) in gastric cancer tissues and its association with clinicopathological characteristics and prognosis of gastric cancer patients. Methods A total of 117 clinical data of gastric cancer patients who underwent surgery in the Central Hospital of Wuhan from October 2013 to October 2014 were retrospectively analyzed. The expression of SIRT4 protein in gastric cancer tissues and its paracancerous tissues were detected by immunohistochemistry, and the associations with SIRT4 expression level and the clinicopathological characteristics and prognosis of gastric cancer patients were analyzed. Results The expression level of SIRT4 protein in gastric cancer tissues was lower than that in paracancerous tissues[(2.138±1.306) points vs (9.582±3.243) points, t=19.078, P<0.001], and the expression of SIRT4 protein was significantly correlated with the tumor differentiation, tumor invasion, lymph node metastasis, lymphovascular invasion, perineural invasion, and TNM stage(all P<0.05). The overall survival rate of SIRT4 low expression group was significantly lower than that of SIRT4 high expression group(P=0.001). Multivariable Cox analysis showed that SIRT4 protein low expression was an independent risk factor affecting the overall survival of gastric cancer patients(HR=2.241, 95%CI:1.252-4.165, P=0.021). Conclusion SIRT4 is lowly expressed in gastric cancer tissues and associated with poor prognosis of gastric cancer patients, which may be a potential prognostic evaluation marker for gastric cancer patients.
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    Value of the combined detection of pepsinogen,gastrin-17 and NEDD9 in the diagnosis of gastric cancer
    WANG Hui, ZHANG Sisen, XU Xiaoyan, MENG Jingjie, MEN Yingli, WEI Tiantian, YANG Jinhua
    2021, 13 (1):  71-75.  doi: 10.3969/j.issn.1674-5671.2021.01.13
    Abstract ( 310 )   PDF (1823KB) ( 136 )   Save
    Objective To investigate the value of the combined detection of pepsinogen(PGⅠ, PGⅡ), gastrin-17(G-17) and neural precursor cell expressed developmentally down-regulated 9(NEDD9) in the diagnosis of gastric cancer. Methods The serum samples of 95 cases of patients with gastric cancer(gastric cancer group) and 140 patients with gastritis(gastritis group) from January 2018 to December 2018 in the People′s Hospital of Zhengzhou were collected, and another 100 healthy subjects in the same period were selected as normal control group. The levels of PGⅠ, PGⅡ, G-17 and NEDD9 were detected by enzyme linked immunosorbent(ELISA). The diagnostic efficiency was evaluated by receiver operating characteristic(ROC) curve analysis and the combined detection of predictors were calculated by logistic regression. Results The expression level differences of PGⅠ, G-17 and NEDD9 between the gastric cancer group and the normal control group were statistically significant(all P<0.05); The PG Ⅱ expression level difference between the gastritis group and the normal control group were statistically significant(P<0.05).The expression levels of G-17 and NEDD9 in early gastric cancer were lower than those in advanced gastric cancer(both P<0.05). The area under the ROC curve(AUC) of PGⅠ, PG Ⅱ, G-17 and NEDD9 in the diagnosis of gastric cancer were 0.664, 0.570, 0.602, 0.749, respectively, and the joint detection of AUC was 0.827, the corresponding sensitivity and specificity were 80.0% and 72.9%, respectively. Conclusion The combined detection of PGⅠ, PGⅡ, G-17 and NEDD9 can improve the diagnosis efficiency of gastric cancer.
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     A study of human serum preparation methods for metabolomic analysis based on liquid chromatography-mass spectrometry
    LI Qianqian, REN Guanhua, YE Chunhua, WU Longjunyu, LI Yuandong, ZHANG Chunyan
    2021, 13 (1):  75-80.  doi: 10.3969/j.issn.1674-5671.2021.01.1
    Abstract ( 1000 )   PDF (37473KB) ( 411 )   Save
    Objective To establish a stable, reliable and suitable preparation method of serum metabolomics for the analysis of large samples. Methods The ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry(UPLC-QTOF-MS) method was utilized to comparatively analyze the preparation methods of human serum for metabolomic analysis, including direct three-fold acetonitrile precipitation(Method 1), concentration and reconstitution after three-fold acetonitrile precipitation(Method 2), and one-fold acetonitrile precipitation(Method 3), and then the biological quality control sample was used to investigate the precision, stability and repeatability of instruments. Results In ESI+ and ESI- scanning, Method 2 yielded the largest characteristic number of metabolites, Method 1 yielded the least number, and Method 3 was in between. No statistically significant difference in the mean peak intensity of the ion peaks was found between Method 1 and Method 3 in the ESI+ and ESI- scanning (all P>0.05), but the results of both methods were greater than that of Method 2 (all P<0.05). The peak intensity coefficient of variation(CV) values of the most ion peaks of Method 2 and Method 3 were less than 25.00%, whereas that of Method 1 was more than 25.00%. The results indicated that the metabolite extraction of Method 3 had better repeatability, and this method could guarantee the proper detection of both the total characteristic number and the peak intensity of metabolites. The precision, stability and repeatability of the instrument during the experiment were all good. Conclusion The serum preparation method that protein molecules are first one-fold acetonitrile precipitated and then intercepted through the ultrafiltration tube can comprehensively retain and detect small molecule compounds in serum samples with a simple and nice reproducible way, and is suitable for metabolomics research.
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    The clinical value of 3.0T MR DWI in differentiating benign and malignant retropharyngeal lymph nodes
    LIANG Jiuping, FU Nianxia, CHEN Huimei, YAN Yaoyao, PENG Huarong, SONG Jianxun
    2021, 13 (1):  81-84.  doi: 10.3969/j.issn.1674-5671.2021.01.15
    Abstract ( 222 )   PDF (4126KB) ( 159 )   Save
    Objective To investigate the clinical value of 3.0T MR diffusion weighted imaging(DWI) in differentiating benign and malignant retropharyngeal lymph nodes. Methods The clinical and imaging data of 44 patients with retropharyngeal lymph nodes RLNs were collected. All of the patients underwent MRI examination, and were divided into benign group(13 cases) and malignant group(31 cases) according to pathological biopsy. The DWI signal and apparent dispersion coefficient(ADC)value were compared, and the receiver operating characteristic(ROC) curve was used to calculate the optimal critical value of ADC and area under the curve(AUC), to evaluate the diagnostic efficacy and to analyze the difference of signal and ADC value of different malignant lymph nodes. Results A total of 65 lymph nodes in the posterior lateral pharyngeal group of 44 patients were included in the analysis, the ADC values of benign group(23 nodes) and malignant group(42 nodes) were(0.833±0.095)×10-3 mm2/s and(0.737±0.136)×10-3 mm2/s , respectively, and the difference was statistically significant(P=0.004). The ADC value of 65 lymph nodes(both benign and malignant) were used to determine benign and malignant lymph nodes and draw ROC curve, and AUC was 0.756. With 0.769×10-3 mm2/s as the best diagnostic cut-off value, the sensitivity for the diagnosis of benign and malignant was 78.3%, and the specificity was 64.3%. The ADC values of the malignant lymph nodes in the signal uniform group and the inhomogeneous group were(0.688±0.092)×10-3 mm2/s and(0.787±0.156)×10-3 mm2/s, respectively, and the difference was statistically significant(P= 0.016). The ADC values of the maximum short diameter of malignant lymph nodes ≤10 mm goup and >10 mm group were(0.745±0.146)×10-3 mm2/s and(0.731±0.131)×10-3 mm2/s, respectively , and the difference was not statistically significant(P=0.748). Conclusion The ADC value of 3.0T MR DWI is an important reference for the differential diagnosis of benign and malignant postpharyngeal lymph nodes. Moreover, DWI can further improve the detection rate of small metastatic retropharyngeal lymph nodes with the maximum short diameter <5 mm.
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    Simultaneous multiple primary carcinomas with liver metastasis:  a case report and literature review
    BAI Yinyin, XU Xinxin, LU Ling, GAN Huizhu
    2021, 13 (1):  85-88.  doi: 10.3969/j.issn.1674-5671.2021.01.16
    Abstract ( 284 )   PDF (3054KB) ( 232 )   Save
    Objective To investigate the etiology, diagnosis and treatment options of simultaneous multiple myeloma and colon cancer. Methods The clinical data of 1 case of the multiple myeloma and colon cancer patient with secondary liver metastasis were retrospectively analyzed, and the relevant literature was reviewed. Results Anemia was the first symptom of the patient, and multiple myeloma was indicated by bone marrow aspiration. The positive of 14q32 IgH gene rearrangement was revealed by fluorescence in situ hybridization, the colon cancer was diagnosed by colonoscopy and pathological biopsy, and the space occupying liver lesion was found a few months later. The colon cancer resection surgery was performed after VTD regime relieved the bone marrow load, then VTD and XELOX combined chemotherapy was performed postoperatively, and local radiofrequency ablation of liver lesions was performed for liver occupying space, the patient could tolerate it, and the liver metastases were significantly smaller than before. Conclusion Simultaneous multiple myeloma and colon cancer with liver metastasis are rare, the histopathology examination is necessary for differential diagnosis of primary and metastatic carcinoma, the treatment of which has not been standardized, the therapeutic plan need to be developed by the multidisciplinary assessment.

     

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     Circulating exosomes PD-L1 and malignant tumors
    ZHANG Wuwen, WANG Fubing
    2021, 13 (1):  89-93.  doi: 10.3969/j.issn.1674-5671.2021.01.17
    Abstract ( 399 )   PDF (7334KB) ( 124 )   Save
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    Research progress of photodynamic therapy for hypoxic tumors
    ZHANG Yu, SU Danke
    2021, 13 (1):  100-105.  doi: 10.3969/j.issn.1674-5671.2021.01.19
    Abstract ( 489 )   PDF (709KB) ( 416 )   Save
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