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1. |
Serum Markers of Bone Metastases in Postmenopausal Breast Cancer Patients Treated with Formestane |
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Tumor Biology,
Volume 18,
Issue 4,
1997,
Page 197-205
Antonia Martinetti,
Emilio Bajetta,
Ettore Seregni,
Nicoletta Zilembo,
Leonardo Ferrari,
Cristina Noberasco,
Simonetta Massaron,
Lorenza Rimassa,
Emilio Bombardieri,
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摘要:
Bone metabolism marker evaluation is expected to play an auxiliary role in the diagnosis and follow-up of bone metastases in patients affected by different types of neoplasms. In this study we have evaluated osteoblastic and osteoclastic markers in 18 patients with bone metastases from breast cancer at diagnosis and for 1 year of follow-up during treatment with the aromatase inhibitor formestane. Osteoblastic markers include the carboxy-terminal propeptide of type I procol-lagen, the bone-specific alkaline phosphatase and the bone GLA protein. The carboxy-terminal cross-linked telopeptide of type I collagen (ICTP) was evaluated as a marker of osteoclastic activity. The patients were classified into three groups according to clinical response. A good correlation between marker level modifications and clinical evolution of skeletal metastases was observed for all the examined markers. Patients with progressive disease showed increasing levels of all markers, whereas patients in regression showed a reduction compared to the basal levels; patients with stable disease fell in between these two categories. We also found that basal ICTP values have prognostic significance: in the stable and progressive disease group they were higher than in the partial response group.
ISSN:1010-4283
DOI:10.1159/000218030
出版商:S. Karger AG
年代:1997
数据来源: Karger
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2. |
Expression of E-Cadherin and α- and β-Catenin mRNAs in Uterine Cervical Cancers |
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Tumor Biology,
Volume 18,
Issue 4,
1997,
Page 206-212
Jiro Fujimoto,
Satoshi Ichigo,
Reiko Hirose,
Hideki Sakaguchi,
Teruhiko Tamaya,
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摘要:
To show the mRNA expressions of E-cadherin and α- and β-catenin – which mainly compose the adherens junction – associated with invasion and metastasis of uterine cervical cancers, we studied the expression of E-cadherin and α- and β -catenin mRNAs in cancers in comparison with normal counterparts. The integral expression of E-cadherin and α- and β -catenin mRNAs was suppressed in the metastatic lesions of advanced uterine cervical cancers, while it was not in the primary tumors. Therefore, the suppressed expression of main adhesion molecules in the adherens junction might contribute to adherens-junctional dysfunction, which might lead to inva-siveness and metastatic potential of advanced uterine cervical cancers as one rate-limi
ISSN:1010-4283
DOI:10.1159/000218033
出版商:S. Karger AG
年代:1997
数据来源: Karger
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3. |
Tumoricidal Activity of Antiseptics with Assessment of Cell Viability in Mice with Severe Combined Immunodeficiency |
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Tumor Biology,
Volume 18,
Issue 4,
1997,
Page 213-218
G. Basha,
F. Penninckx,
K. Geboes,
P. Yap,
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摘要:
Previously, we have assessed the efficacy of different cytotoxic agents on the viability of SW620 human colonic carcinoma cells in vitro. In this study, we have investigated the tumoricidal efficacy of some antiseptic agents on SW620 human colonic carcinoma cells which were subsequently inoculated into severe combined immunodeficient (SCID) mice. An inoculum of 5 × 106 cells suspended in 200 μl buffer solution was found to be the minimum number of cells needed to result in tumour growth within 8 weeks after subcutaneous injection into SCID mice. The integrity of the cells was assessed in vitro with the trypan blue exclusion test after 30 min incubation in distilled water (DW), chloramine 0.5% in DW and polyvinyl pyrrolidone iodine (PVP-I) 0.01, 0.05, 0.1 and 5% in DW. DW and PVP-I 0.01% were not tumoricidal, neither in vitro nor in vivo. In contrast, PVP-I 5% and chloramine 0.5% ‘killed’ all or almost all tumour cells in vitro and prevented their growth in vivo. PVP-I 0.05 and 0.1% were less effective in vitro than 5 %, but could prevent in vivo proliferation unless an adjustment of the residual number of viable tumour cells was performed. These data indicate the importance of the amount of the tumour inoculum and hence the need to use a maximally effective ‘killing
ISSN:1010-4283
DOI:10.1159/000218034
出版商:S. Karger AG
年代:1997
数据来源: Karger
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4. |
Regulation of Gelatinase Production and Invasiveness by Organ-Specific Fibroblasts in High- and Low-Metastatic Clones from Murine RCT Sarcoma |
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Tumor Biology,
Volume 18,
Issue 4,
1997,
Page 219-231
Kazuo Ohmori,
Hisao Matsui,
Masahiko Kanamori,
Kazuo Yudoh,
Taketoshi Yasuda,
Haruo Tsuji,
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摘要:
Regulation of gelatinase production, invasiveness and migration activity by organ-specific fibroblasts from embryo, subcutaneous and lung tissues of mice were investigated in high-metastatic RCT+ and low-metastatic RCT- clones established from a poorly differentiated murine sarcoma. In the conditioned media of RCT+ cells, mouse skin fibroblasts (MSF) obtained from the tissue of tumor origin (orthotopic) stimulated the production of the 105-kD gelatinase more than C3H/ 10T1/2 clone 8 (C3H/10T1/2 CL8) or mouse lung fibroblasts (MLF). In the conditioned media of RCT- cells, however, cocultivation with fibroblasts showed only slight stimulatory effects on the production of the 105-kD gelatinase. In the invasion assay, using a reconstituted basement membrane (matri-gel), RCT+ cells cocultivated with MSF showed significantly higher invasiveness than those cocultivated with C3H/10T1/2 CL8 or MLF. However, no significant differences were shown in the invasiveness of RCT- cells in cocultivation with three types of fibroblasts and in cultivation without fibroblasts. There was no significant difference in migration activity between RCT+ and RCT- cells cultivated alone. But in the cocultivation of both clones with MSF, the migration activity of RCT+ cells was significantly higher than that of RCT- cells. These findings suggest that MSF might delineate the difference in characteristics related to the metastatic potential of RCT+ and RCT- cells through regulation by organ-specific factors.
ISSN:1010-4283
DOI:10.1159/000218035
出版商:S. Karger AG
年代:1997
数据来源: Karger
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5. |
Effect of Paclitaxel (Taxol®) on CA 125 Expression and Release by Ovarian Cancer Cell Lines |
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Tumor Biology,
Volume 18,
Issue 4,
1997,
Page 232-240
J.M.G. Bonfrer,
T.C. Linders,
P.C. Hageman,
J.G.W. Hilkens,
C.M. Korse,
C.F.M. Molthof,
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摘要:
Two ovarian cancer cell lines, OVC432 and the newly established CVU4I, were used to study the effect of Taxol on cell growth and simultaneous CA 125 antigen expression. Growth of both cell lines was effectively inhibited by drug concentrations of 0.1 µM and higher. Complete inhibition of cell growth may result from high concentrations of Cremophor EL present in the Taxol formulation. Immunohistochemical analysis demonstrated that both cell lines retained the CA 125 expression on the cell surface during exposure to paclitaxel. This was reflected in a constant statistically significant correlation between cell numbers and CA 125 concentrations found in cell lysates. CA 125 levels in the culture medium showed a significant relation to cell numbers and, consequently, to the response of the cell line to the administered anticancer drug. It may be concluded from this study that CA 125 seems to be a reliable tumor marker in monitoring tumor response during paclitaxel treatment
ISSN:1010-4283
DOI:10.1159/000218036
出版商:S. Karger AG
年代:1997
数据来源: Karger
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6. |
Prognostic Significance of Tumour Markers in Endometrial Cancer |
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Tumor Biology,
Volume 18,
Issue 4,
1997,
Page 241-249
S.S.T. Lo,
D.K.L. Cheng,
T.Y. Ng,
L.C. Wong,
H.Y.S. Ngan,
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摘要:
Serum cancer antigen (CA) 125, CA15.3, CA19.9, carcinoembryonic antigen and tissue polypeptide antigen were analyzed in 100 normal subjects, 47 patients with benign gynaecological diseases and 97 patients with endometrial cancer. The incidence of individual elevated tumour markers ( > 2SD) was 21.5–30.9% in cancer patients. Elevations of CA125 and CA15.3 were significantly associated with poor prognostic clinical factors. Univariate anaylses showed that elevated CA125, CA15.3 and CA19.9 were significantly associated with shorter survival. In multivariate analyses, CA15.3 was highly significant and had a larger hazard ratio. In conclusion, CA15.3 is a useful marker for the prognosis of patients with endometrial cance
ISSN:1010-4283
DOI:10.1159/000218037
出版商:S. Karger AG
年代:1997
数据来源: Karger
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7. |
Hyperthermia Potentiates Antitumor Effect of Thermosensitive-Liposome-Encapsulated Melphalan and Radiation in Murine Melanoma |
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Tumor Biology,
Volume 18,
Issue 4,
1997,
Page 250-260
Tamiz P. Chelvi,
Ranju Ralhan,
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摘要:
Malignant melanoma are chemoresistant tumors with poor prognosis. The aim of this study was to determine whether multimodality therapy of murine melanoma involving a combination of radiation with thermosen-sitive-liposome-encapsulated melphalan and local hyperthermia would result in enhancement of therapeutic efficacy for a more effective management of melanoma. Melphalan was entrapped in thermosensitive liposomes prepared from natural lipids: egg phosphatidyl choline, cholesterol and ethanol to show phase transition at 42 ± 0.5° C and used in combination with localized heating of B16F10 murine melanoma transplanted into the legs of C57B1/6 mice for selective drug targeting at the tumors and/or radiation for treatment of melanoma. Murine melanoma transplanted into C57B1/6 mice were subjected to bimodality treatments involving a combination of radiation, hyperthermia or melphalan. Partial tumor regression was observed in mice receiving a combination of hyperthermia and radiation (median tumor volume 427.3 mm3) or a combination of free melphalan and radiation (512.1 mm3) as compared to untreated controls (630.9 mm3). Each group consisted of 18 animals, and the results are expressed as median tumor volume ± SD. Animals receiving multimodality therapy comprising irradiation followed by injection of thermosensitive liposomal melphalan and hyperthermic treatment of the tumor-bearing leg at 42 ± 0.5°C for 1 h showed marked tumor regression in comparison with untreated controls or animals treated with a combination of radiation and hyperthermia or radiation and free-drug melphalan. Animals receiving thermoradiochemotherapy also showed prolonged survival; 70% of animals survived for more than 3 months. The study shows greater tumor cell killing, tumor growth delay and prolonged survival produced by a combination of radiation, thermosensitive-liposome-entrap-ped melphalan and hyperthermia compared with animals receiving single-modality or bimodality treatments. It is concluded that this multimodality approach will be potentially useful for more effective management of mela
ISSN:1010-4283
DOI:10.1159/000218038
出版商:S. Karger AG
年代:1997
数据来源: Karger
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