OBJECTIVE: To evaluate the clinicopathological implications of Rb pathway alteration and E2F-1 expression in Epithelial ovarian cancer using immunohistochemical staining. METHODS: Tissue samples (n=72) were collected after staging operation between 1998 and 2004. RESULTS: In 72 cases, the overall expression of pRb, and E2F-1 were 59.7% (43/72), and 58.3% (42/72), respectively. pRb expression was inversely correlated with stage, histologic grade and mitotic index. E2F-1 expression was correlated with advanced stages, high grade, mitotic index, Ki-67 labeling index (LI). CONCLUSION: We suggest that Rb pathway alteration and E2F-1 expression could play roles as a new prognostic factors in Epithelial ovarian cancer.
Mitotic Index ; Ovarian Neoplasms*

OBJECTIVE: To find out the optimal conditions of human chromosomal analysis protocol in peripheral blood sample. METHODS: The experiments were made with the variations of phytohaemagglutinin, colcemid, ethidium bromide concentration and the variations of hypotonic solution exposure time. RESULTS: In the experiment on the optimal phytohaemagglutinin concentration, the highest mitotic index in the overall collected cells was obtained in phytohaemagglutinin concentration 15microL/ml. In the experiment on the concentration of mitotic arrestant colcemid, the proper chromosomal state that is meta phase stage and doesn't have many chromosomal crossings or tangles was obtained in colcemid concentration 0.05microg/ml. In the experiment on the optimal exposure time of hypotonic solution(0.075M KCl) treatment, the most suitable intervals between chromosomes were subtained in 20 minutes. In the experiment on the optimal concentration of ethidium bromide to obtain minute chromosomal bands, the best result was when ethidium bromide concentration 5microg/ml or 7.5microg/ml was addition to colcemid concentration 0.02microg/ml. CONCLUSION: The combination of phytohaemagglutinin 15microL/ml, colcemid 0.05microg/ml, hypotonic solution exposure time for 20 minutes is important to the collection of appropriate chromosome state in human chromosomal analysis using peripheral blood. In the case that needs to obtain minute bands, the elongated chromosomes are obtained when ethidium bromide 5microg/ml or 7.5microg/ml in addition to colcemid concentration 0.02microg/ml with the same conditions of phytohaemagglutinin and hypotonic solution.
Demecolcine ; Ethidium ; Humans ; Mitotic Index

BACKGROUND: Peripheral blood is the most frequently used specimen for routine chromosome analysis. The classical method using flask for cell culture needs a lot of reagent and is cumbersome. To simplify the procedure, we tried using culture tube and modifying the fixation method. The purpose of this study is to assess the reliability of the modified method using culture tube for chromosome analysis of peripheral blood. METHODS: We tested peripheral blood of ten normal healthy persons. In the modified method, culture tube (110 mm 16 mm, Nunc, Roskilde, Denmark) containing 2.25 mL RPMI 1640 supplemented with fetal calf serum and phytohemagglutinin was used. Harvest was done in the culture tube. Fixative 2.0 mL was added without centrifugation after hypotonic treatment. After 10 min incubation at room temperature, the cells were pelleted and washed. This method was compared with the reference method using flask. We evaluated the quality of chromosome and calculated mitotic index. RESULTS: Chromosome quality of the modified method using culture tube was good and the same as that of the reference method. Mitotic index was higher in the modified method (1.0~4.3%, mean 2.5%) than in the reference method (0.4~2.2%, mean 1.2%) (P<0.01). CONCLUSIONS: The modified method needs less amount of reagent and is easy to do. The chromosome quality was good enough to evaluate the karyotype. So, this modification enable to improve the effectiveness of chromosome laboratory.
Cell Culture Techniques ; Centrifugation ; Humans ; Karyotype ; Mitotic Index

There are few reports of gastrointestinal stromal tumors (GISTs) in the esophagus. The authors report a patient with an esophageal GIST that was found incidentally during an endoscopy. The endoscopy revealed a 1 cm sized mass with a granular surface at the 32 cm site from the upper incisor. Endoscopic ultrasonography revealed the tumor to be located in the muscularis mucosa of the esophageal wall. Histologically, the tumor consisted of spindle cells, with no mitotic index, that were immunoreactive for KIT and S-100. The tumor was diagnosed as a gastrointestinal stromal tumor with neural differentiation (GINT). An endoscopic mucosal resection was performed and the patient has been on routine follow up at the out patient department for three months.
Endoscopy ; Endosonography ; Esophagus ; Follow-Up Studies ; Gastrointestinal Stromal Tumors* ; Humans ; Incisor ; Mitotic Index ; Mucous Membrane

BACKGROUND: Immature teratoma (IT) is a tumor containing immature neuroectodermal tissue, primarily in the form of neuroepithelial tubules. However, the diagnosis of tumors containing only cellular neuroglial tissue (CNT) without distinct neuroepithelial tubules is often difficult, since the histological characteristics of immature neuroectodermal tissues remain unclear. Here, we examined the significance of CNT and tried to define immature neuroectodermal tissues by comparing the histological features of neuroglial tissues between mature teratoma (MT) and IT. METHODS: The histological features of neuroglial tissue, including the cellularity, border between the neuroglial and adjacent tissues, cellular composition, mitotic index, Ki-67 proliferation rate, presence or absence of tissue necrosis, vascularity, and endothelial hyperplasia, were compared between 91 MT and 35 IT cases. RESULTS: CNTs with a cellularity grade of ≥ 2 were observed in 96% of IT cases and 4% of MT cases (p < .001); however, CNT with a cellularity grade of 3 in MT cases was confined to the histologically distinct granular layer of mature cerebellar tissue. Moreover, CNT in IT exhibited significantly higher rates of Ki-67 proliferation, mitoses, and necrosis than those in MT (p < .001). Furthermore, an infiltrative border of neuroglial tissue and glomeruloid endothelial hyperplasia were significantly more frequent in IT cases than in MT cases (p < .001). CONCLUSIONS: Our results suggest that if CNT with a cellularity grade of ≥ 2 is not a component of cerebellar tissue, such cases should be diagnosed as IT containing immature neuroectodermal tissue, particularly if they exhibit an infiltrative border, mitoses, necrosis, and increased Ki-67 proliferation.
Diagnosis ; Female ; Hyperplasia ; Mitosis ; Mitotic Index ; Necrosis ; Neural Plate ; Neuroglia ; Ovary ; Teratoma*

Mitomycin C was introduced to human leukocyte cultures to investigate the analysis of chromosome aberration by G-banding patterns. The relationship between mitomycin C and secondary constriction; length of treatment and exposure time of the compound; and G-banding pattern were discussed. The results are summarized as follows: 1. The mitotic rate of cultures exposed to mitomycin C at a concentration of 0. 1 microgram/ml for 24 hours did not inhibit significantly compared with that of the control, and chromosome aberrations were relatively very low. However, the mitotic index of cells exposed to 1.0 microgram/ml for 1 hour or 24 hours was significantly below the control index and a relatively high number of aberrations were found. With the concentration of 0.5 microgram/ml for the last 24 hours of cultural incubation, there was little inhibition of mitotic activity and the highest frequency of observable aberrations were found. Thus, in this study, treatment of the concentration of 0.5 microgram/ml for the last 24 hours of cultures proved to be the most efficient combination for examining the effect of this compound on human leukocyte chromosomes. 2. Mitomycin C did not appear to break the chromosome randomly. More than half of the aberrations were of the interchange type which were in most cases involved with chromosomes 1, 9 and 16. They are joined in, at least, the secondary constrictrion regions of one of these chromosomes. The secondary constriction regions contain 60 to 70 percent of the total breaks of each of these chromosomes. The other types of chromosome aberrations were simple chromatid and chromosome breaks at the interband of G-bands and translocations. The frequent association of satellites with 2 to 5 acrocentric chromosomes was also observed. In conclusion, it can be stated that mitomycin C is very specific in causing lesions to appear at the secondary constriction of human chromosomes 1, 9 and 16. The dosage of mitomycin C, length of treatment and exposure time during the culture period are very important factors for induction of chromosome abnormalities, which vary with the individual's leukocytes that have different genetic constitutions.
Chromosome Aberrations* ; Female ; Human ; Karyotyping ; Male ; Mitomycins/adverse effects* ; Mitotic Index ; Staining and Labeling

Sister chromatid exchanges(SCEs) and cell cycle kinetics were proposed as a sensitive and quantitative assay for mutagenicity and cytotoxicity in short-term cultures of phytohemagglutinin(PHA)-stimulated human lymphocytes. Therefore, this study was performed to investigate the relation between the cytotoxic effects and sister chromatid exchanges. The results are summarized as follows: 1) The frequency of SCEs per cell are 13.1+/-2.8 in the lower concentration of 6.25x10(-9) M and 75.8+/-8.2 in the highest concentration of 1.00+/-10(-7) M. Mitotic index is decreased in the higher concentration of mitomycin C. The result indicates that mitomycin C led to a dose dependent increase in SCE frequency, but decrease in mitotic index. 2) Chromosomal analysis was performed on metaphase cells that have divided one, two, and three or more times for cell cycle kinetics by fluorescence-plus-Giemsa(FPG) technique. According to the increased but the cells of third division are greatly decreased. 3) The frequency of SCEs per chromosome by chromocomal group are decreased gradually from A group to G group. But relationships between specific chromosomal group and SCEs frequency are not found.
Cell Cycle ; Chromatids ; Humans ; Humans* ; Kinetics ; Lymphocytes ; Metaphase ; Mitomycin* ; Mitotic Index ; Siblings* ; Sister Chromatid Exchange*

PURPOSE: The mitotic index (MI) and Ki-67 labeling index have been used as cell proliferative markers in the various tumors. Topoisomerase II alpha (Topo II alpha) is also expressed in proliferating cells. The aim of this study was to evaluate the correlations between the MI, Ki-67, and Topo II alpha expression as proliferative markers of breast cancer. METHODS: The cell proliferative activity of 181 breast cancers was measured using MI, Ki-67 labeling index and Topo II alpha expression. The correlation between the measured markers was also analyzed. RESULTS: The MI, Ki-67, and Topo II alpha were significantly correlated with each other(p < 0.000). The MI and Ki-67 labeling index were associated with high histological grade, and absence of hormone receptor (p < 0.000). Topo II alpha expression was correlated with high histological grade (p < 0.000), absence of hormone receptor and HER-2/neu overexpression (p < 0.043). The MI, Ki-67, and Topo II alpha were not associated with any other clinical variables, such as age, tumor size, and lymph node status. CONCLUSION: The three proliferative indices were significantly associated with aggressive features of breast cancer, and significantly correlated with each other.
Breast Neoplasms* ; Breast* ; DNA Topoisomerases, Type II ; Lymph Nodes ; Mitotic Index

Meningiomas are common brain tumors that show a predilection for females and become more aggressive during pregnancy and menses. Clinical and epidemiological observations regarding meningiomas suggest a sex hormone dependency of these tumors. We reviewed the 47 intracranial meningiomas to examine the presence of the progesterone receptor(PR) by immunohistochemical methods and the relationships between the PR immunostaining status and other parameters, such as age, sex, tumor grade, mitotic index, and Ki-67 staining index. The PR staining status in these tumors was analyzed by immunohistochemistry on formalin-fixed paraffinembedded archival tissue sections utilizing the monoclonal antibody. The results are summarized as follows: 1) fifteen tumors(31.9%) tested were positive for the PR, 2) patients age and sex had no significant relationship with the PR positive rate of meningiomas(p=0.680, and 0.968, respectively), 3) although the positive immunostaining rate for the PR in benign meningiomas(37%) was higher than that in atypical and malignant meningiomas(25%), there was no statistically significant difference between these two groups(p=0.381), and 4) proliferative potentials such as the Ki-67 staining index and the mitotic index were not correlated with the PR staining status(p=0.4578 and 0.1981. respectively). We believe that further studies using large series of patients are needed to elucidate the role of the PR in meningiomas.
Brain Neoplasms ; Female ; Humans ; Immunohistochemistry ; Meningioma* ; Mitotic Index ; Pregnancy ; Progesterone* ; Receptors, Progesterone*

An abnormally enlarged right ovary and a mass in fat surrounding the right kidney were discovered in a dairy cow during routine postmortem examination at slaughter. The ovary was dark reddish and multinodular in shape. Numerous cystic structures were identified in the mass. Histopathologically, the ovary was completely replaced with large, uniform, polyhedral neoplastic cells containing vesicular nuclei and prominent nucleoli. The mitotic index was high. In the lymphatic vessels, tumor emboli were observed. Another mass in the fat surranding the right kidney had the same histological features as the ovarian mass. This animal was diagnosed with malignant dysgerminoma and metastasis to other peritoneal organs.
Animals ; Autopsy ; Dysgerminoma* ; Female ; Kidney ; Lymphatic Vessels ; Mitotic Index ; Neoplasm Metastasis ; Ovary