Objective： The aim of this study was to investigate the MRP-1/CD9mRNA expression in lung cancer and normal lung tissues and the relationship between its expression and pathologic grades, clinical stages, metastasis a...Objective： The aim of this study was to investigate the MRP-1/CD9mRNA expression in lung cancer and normal lung tissues and the relationship between its expression and pathologic grades, clinical stages, metastasis and prognosis. Methods： To observe MRP-1/C9mRNA expression, tissue microarray （TMA） containing 54 lung cancers and 10 normal lung tissues was prepared and Fluorescence in situ hybridization was used. Results： The positive rate of MRP-1/CD9 expression was 48.1% in lung cancer, lower than that of normal lung tissues. The statistical difference was significant （P〈0.05）. Its protein expression had no relationship with the patients＇ ages, sex and the macroscopic type of tumor, but had relationships with the histological type, clinical stage, differentiated degree and metastasis. The expression in non-small cell lung cancer （NSCLC） was higher than that in small cell lung cancer （SCLC）; in well-moderately differentiated group was higher than that in poorly differentiated group; Earlier period group （I＋II） was higher than in later period group （Ⅲ＋Ⅳ）; and in group without lymphoid metastasis was higher than in patients with lymphoid metastasis. Conclusion： The progression of the lung cancer maybe related with the descended MRP-1/Cd9 expression, which may be useful in evaluating the prognosis of cancer patients.展开更多
Object: To localize the mRNA coding for VEGF at Ultrastractural level in human breast cancer by using digoxigenin-labeled cDNA probes. Methods: Nonradioactive in situ hybridization at electron microscopic level was em...Object: To localize the mRNA coding for VEGF at Ultrastractural level in human breast cancer by using digoxigenin-labeled cDNA probes. Methods: Nonradioactive in situ hybridization at electron microscopic level was employed to detected VEGF mRNA in breast cancer. Result: Cancer cells and endothelial cell of angiogensis show dark color in experiment sections. No dark color can be found in control sections. Positive hybridization signals showed dark dot and were located in various compartments of the breast cancer cell and endothelial cell in experiment section. No labeling was observed in control sections. In experiment sections, the staining appeared concentrated in cytoplasm and nucleus of the breast cancer cell and endothelial cell. Conclusion: Nonradioactive in situ hybridization at electron microscopic level is efficient for direct observation of the target site mRNA of VEGF in the cytoplasm and nucleus.展开更多
Previous immunohistochemical studies showed that the human placenta contained notonly many regulatory peptides, but also 5-HT and dopamine (DA) classicalneurotransmitters. These results made us suggest the following h...Previous immunohistochemical studies showed that the human placenta contained notonly many regulatory peptides, but also 5-HT and dopamine (DA) classicalneurotransmitters. These results made us suggest the following hypothesis: the human placentamight be a complex endocrine organ. In order to confirm this hypothesis, it must beunderstood whether these regulatory peptides and classical neurotransmitters can be pro-展开更多
get insight on the regulatory mechanism of Ki 67 gene expression in malignant cell cycle MethodsNon radioactive in situ hybridization (ISH) was undertaken, combined with immunohistochemistry to study the Ki 67 gene tr...get insight on the regulatory mechanism of Ki 67 gene expression in malignant cell cycle MethodsNon radioactive in situ hybridization (ISH) was undertaken, combined with immunohistochemistry to study the Ki 67 gene transcription and translation in various human cells and tissues HeLa cells and fresh colon cancer cells, tonsil, normal pancreas and pancreatic cancer tissues were used in this study A 435?bp cDNA fragment located in exon 13 of the Ki 67 antigen gene was amplified by polymerase chain reaction (PCR) Digoxigenin labelled antisense and sense RNA probes were prepared for detecting Ki 67 mRNA, combined with MIB 1 immuno^histochemistry Results Successful localization of Ki 67 mRNA in human HeLa cells, colon cancer cells, tissues specimen of the tonsil and pancreatic cancer tissue sections was accomplished by digoxigenin labelling in situ hybridization technique ISH to colon cancer cells and pancreatic cancer tissue slides showed that much stronger cytoplasm and perinuclear mRNA signals of the Ki 67 gene were present in malignant cells than in normal cells, which was in accordance with MIB 1 nuclear protein signals Conclusions A sensitive and practical in situ hybridization method for the analysis of Ki 67 antigen mRNA in human cell and tissue was developed Abnormal transcription of exon 13 of Ki 67 gene might be responsible for malignant cell proliferation in colon and pancreatic展开更多
In this research, we investigated the expression of C myc and N-ras mRNAs on 21 cases paraffin- embedded tissue sections of hepatocellular carcinoma(HCC) using insitu hybridization technique with biotinylated labelle...In this research, we investigated the expression of C myc and N-ras mRNAs on 21 cases paraffin- embedded tissue sections of hepatocellular carcinoma(HCC) using insitu hybridization technique with biotinylated labelled cDNA probes. Of 21 cases of hepatoma , C-myc mRNA was positive-expressed in 9 cases(42. 9 % ) and N-ras positive in 4 cases ( 19% ) in hepatoma cells, and C-myc and N-ras positive in 4 and 1 cases respectively in peritumor hepatocytes. C- myc mRNAs were localized within cytoplasms of both hepatoma cells and peritumor hepatocytes. However , the positive intensities of C-myc and N-ros mRNAs in hepatoma cells were much greater than those in peritumor hepatocytes. The results indicated that Cmyc and N-ras oncogenes were overexpressed in HCC, and may play an important role in coordinatively maintaince of the malignant phenotypes in HCC.展开更多
目的 探讨大鼠消化道是否存在 Gn RH受体 m RNA及其定位。 方法 用原位杂交组织化学法。 结果 胃底腺壁细胞、胃小凹上皮细胞可检测到较强的 Gn RH受体 m RNA杂交信号。3段小肠绒毛上皮细胞、小肠腺细胞可检测到较强的 Gn RH受体 m...目的 探讨大鼠消化道是否存在 Gn RH受体 m RNA及其定位。 方法 用原位杂交组织化学法。 结果 胃底腺壁细胞、胃小凹上皮细胞可检测到较强的 Gn RH受体 m RNA杂交信号。3段小肠绒毛上皮细胞、小肠腺细胞可检测到较强的 Gn RH受体 m RNA杂交信号。盲肠、结肠和直肠的粘膜上皮细胞、肠腺上皮细胞也能检测到 Gn RH受体 m RNA杂交信号。信号物质均分布在胞质内 ,胞核呈阴性。 结论 大鼠消化道能合成 Gn RH受体。Gn RH也是一种胃肠激素 ,它由消化系统自身合成 。展开更多
基金This work was supported by a grant from Tianjin Science and Technology Committee (No. 033804211)
文摘Objective： The aim of this study was to investigate the MRP-1/CD9mRNA expression in lung cancer and normal lung tissues and the relationship between its expression and pathologic grades, clinical stages, metastasis and prognosis. Methods： To observe MRP-1/C9mRNA expression, tissue microarray （TMA） containing 54 lung cancers and 10 normal lung tissues was prepared and Fluorescence in situ hybridization was used. Results： The positive rate of MRP-1/CD9 expression was 48.1% in lung cancer, lower than that of normal lung tissues. The statistical difference was significant （P〈0.05）. Its protein expression had no relationship with the patients＇ ages, sex and the macroscopic type of tumor, but had relationships with the histological type, clinical stage, differentiated degree and metastasis. The expression in non-small cell lung cancer （NSCLC） was higher than that in small cell lung cancer （SCLC）; in well-moderately differentiated group was higher than that in poorly differentiated group; Earlier period group （I＋II） was higher than in later period group （Ⅲ＋Ⅳ）; and in group without lymphoid metastasis was higher than in patients with lymphoid metastasis. Conclusion： The progression of the lung cancer maybe related with the descended MRP-1/Cd9 expression, which may be useful in evaluating the prognosis of cancer patients.
基金This work was supported by NationalNatural Science Foundation of China (No. 39870314).
文摘Object: To localize the mRNA coding for VEGF at Ultrastractural level in human breast cancer by using digoxigenin-labeled cDNA probes. Methods: Nonradioactive in situ hybridization at electron microscopic level was employed to detected VEGF mRNA in breast cancer. Result: Cancer cells and endothelial cell of angiogensis show dark color in experiment sections. No dark color can be found in control sections. Positive hybridization signals showed dark dot and were located in various compartments of the breast cancer cell and endothelial cell in experiment section. No labeling was observed in control sections. In experiment sections, the staining appeared concentrated in cytoplasm and nucleus of the breast cancer cell and endothelial cell. Conclusion: Nonradioactive in situ hybridization at electron microscopic level is efficient for direct observation of the target site mRNA of VEGF in the cytoplasm and nucleus.
文摘Previous immunohistochemical studies showed that the human placenta contained notonly many regulatory peptides, but also 5-HT and dopamine (DA) classicalneurotransmitters. These results made us suggest the following hypothesis: the human placentamight be a complex endocrine organ. In order to confirm this hypothesis, it must beunderstood whether these regulatory peptides and classical neurotransmitters can be pro-
基金boththeNationalNaturalScienceFoundationofChina (No 396 0 0 14 1)andtheNaturalScienceFoundationofZhejiangProvince (No 396 498
文摘get insight on the regulatory mechanism of Ki 67 gene expression in malignant cell cycle MethodsNon radioactive in situ hybridization (ISH) was undertaken, combined with immunohistochemistry to study the Ki 67 gene transcription and translation in various human cells and tissues HeLa cells and fresh colon cancer cells, tonsil, normal pancreas and pancreatic cancer tissues were used in this study A 435?bp cDNA fragment located in exon 13 of the Ki 67 antigen gene was amplified by polymerase chain reaction (PCR) Digoxigenin labelled antisense and sense RNA probes were prepared for detecting Ki 67 mRNA, combined with MIB 1 immuno^histochemistry Results Successful localization of Ki 67 mRNA in human HeLa cells, colon cancer cells, tissues specimen of the tonsil and pancreatic cancer tissue sections was accomplished by digoxigenin labelling in situ hybridization technique ISH to colon cancer cells and pancreatic cancer tissue slides showed that much stronger cytoplasm and perinuclear mRNA signals of the Ki 67 gene were present in malignant cells than in normal cells, which was in accordance with MIB 1 nuclear protein signals Conclusions A sensitive and practical in situ hybridization method for the analysis of Ki 67 antigen mRNA in human cell and tissue was developed Abnormal transcription of exon 13 of Ki 67 gene might be responsible for malignant cell proliferation in colon and pancreatic
文摘In this research, we investigated the expression of C myc and N-ras mRNAs on 21 cases paraffin- embedded tissue sections of hepatocellular carcinoma(HCC) using insitu hybridization technique with biotinylated labelled cDNA probes. Of 21 cases of hepatoma , C-myc mRNA was positive-expressed in 9 cases(42. 9 % ) and N-ras positive in 4 cases ( 19% ) in hepatoma cells, and C-myc and N-ras positive in 4 and 1 cases respectively in peritumor hepatocytes. C- myc mRNAs were localized within cytoplasms of both hepatoma cells and peritumor hepatocytes. However , the positive intensities of C-myc and N-ros mRNAs in hepatoma cells were much greater than those in peritumor hepatocytes. The results indicated that Cmyc and N-ras oncogenes were overexpressed in HCC, and may play an important role in coordinatively maintaince of the malignant phenotypes in HCC.
文摘目的 探讨大鼠消化道是否存在 Gn RH受体 m RNA及其定位。 方法 用原位杂交组织化学法。 结果 胃底腺壁细胞、胃小凹上皮细胞可检测到较强的 Gn RH受体 m RNA杂交信号。3段小肠绒毛上皮细胞、小肠腺细胞可检测到较强的 Gn RH受体 m RNA杂交信号。盲肠、结肠和直肠的粘膜上皮细胞、肠腺上皮细胞也能检测到 Gn RH受体 m RNA杂交信号。信号物质均分布在胞质内 ,胞核呈阴性。 结论 大鼠消化道能合成 Gn RH受体。Gn RH也是一种胃肠激素 ,它由消化系统自身合成 。
