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1.
J BUON ; 16(2): 241-6, 2011.
Article in English | MEDLINE | ID: mdl-21766492

ABSTRACT

PURPOSE: Many of commonly used chemotherapeutics in lung cancer treatment are metabolized by glutathione-S transferases (GSTs). The placental isoform of GST (GSTP1) is the most abundant isoform in the lung. Polymorphisms within the GSTP1 may result in alterations in enzyme activity and change sensitivity to platinum-based chemotherapy. We investigated whether the polymorphism within the exons 5 and 6 of GSTP1 gene may change response to therapy, time to tumor progression (TTP) and overall survival in small cell lung cancer (SCLC) patients. METHODS: Ninety-four histologically confirmed patients with SCLC were enrolled in this study during 1995-2006. GSTP1 Ile105Val polymorphism in exon 5 and GSTP1 Ala- 114Val polymorphism in exon 6 were determined by using PCR-RFLP techniques. Associations between the GSTP1 polymorphisms and treatment response were evaluated using the chi-square test. Associations between the GSTP1 polymorphisms and TTP and overall survival were compared using Kaplan-Meier survival curves. RESULTS: We found no significant associations between exon 5 and exon 6 GSTP1 gene polymorphisms and response to therapy or overall survival. Patients carrying both variant exon 5 (Ile/Val or Val/Val) and variant exon 6 (Ala/Val) genotypes had significantly shorter TTP (5 vs. 8 months, p = 0.04). Moreover, patients with heterozygote exon 6 variant had presented with extensive-stage disease. CONCLUSION: No individual effect of variant alleles was found in relation to chemotherapy response, median TTP and overall survival. The carriage of both types of variant alleles may predict worse outcome.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Glutathione S-Transferase pi/genetics , Lung Neoplasms/genetics , Polymorphism, Single Nucleotide/genetics , Small Cell Lung Carcinoma/genetics , Cisplatin/administration & dosage , Combined Modality Therapy , DNA, Neoplasm/blood , DNA, Neoplasm/genetics , Disease Progression , Etoposide/administration & dosage , Exons/genetics , Female , Genotype , Humans , Lung Neoplasms/blood , Lung Neoplasms/therapy , Male , Middle Aged , Neoplasm Staging , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Radiotherapy , Small Cell Lung Carcinoma/blood , Small Cell Lung Carcinoma/therapy , Survival Rate , Time Factors , Treatment Outcome
2.
Med Oncol ; 28(1): 137-9, 2011 Mar.
Article in English | MEDLINE | ID: mdl-20119689

ABSTRACT

Pancreatic panniculitis (PP) is a rare disease presenting during the course of pancreatic diseases such as acute and chronic pancreatitis, pancreatic carcinoma. There are also a few reports of PP associated with other carcinomas. We present a 69-year-old male patient of gastric carcinoma with PP. The literature is reviewed, clinical and histological features of the case are discussed. This is the first case of PP in a gastric carcinoma patient reported in literature. As a conclusion, PP can be the first manifestation of a pancreatic metastasis of any carcinoma.


Subject(s)
Adenocarcinoma/complications , Pancreatic Diseases/etiology , Panniculitis/etiology , Stomach Neoplasms/complications , Adenocarcinoma/pathology , Aged , Humans , Lipase/metabolism , Male , Pancreatic Diseases/pathology , Panniculitis/pathology , Stomach Neoplasms/pathology
3.
Genet Mol Res ; 9(1): 97-106, 2010.
Article in English | MEDLINE | ID: mdl-20092039

ABSTRACT

Detection of residual tumor cells in the circulation can provide prognostic as well as therapeutic information and help in identifying patients at high risk for developing metastases. Maspin and mammaglobin are two molecules that are specifically associated with breast cancer. We looked for mammaglobin and maspin transcripts in the peripheral blood of patients with breast cancer and evaluated their utility as a marker of the response to therapy. Maspin and mammaglobin transcripts were analyzed in 85 breast-cancer patients by nested RT-PCR, prior to and after treatment. Before therapy, 10 patients were found positive for mammaglobin and 20 patients were positive for maspin. In four patients, both transcripts were detected. Immediately following treatment, only one patient was still positive for mammaglobin while maspin transcripts persisted in three patients. Disease progression was observed mainly in patients in whom maspin transcripts were not detectable. Molecular detection of circulating tumor cells during therapy based on analysis for mammaglobin and maspin transcripts is an easy and practical method that can be applied to follow-up patients. We suggest that detection of mammaglobin mRNA is useful to determine the effect of therapy while maspin transcripts may indicate more aggressive disease.


Subject(s)
Biomarkers, Tumor/blood , Breast Neoplasms/therapy , Neoplasm Proteins/genetics , RNA, Messenger/blood , RNA, Neoplasm/blood , Serpins/genetics , Uteroglobin/genetics , Adult , Biomarkers, Tumor/genetics , Breast Neoplasms/blood , Breast Neoplasms/pathology , Disease Progression , Female , Humans , Mammaglobin A , Middle Aged , Neoplastic Cells, Circulating/metabolism , Neoplastic Cells, Circulating/pathology , Prognosis , Transcription, Genetic
4.
Eur J Gynaecol Oncol ; 30(2): 223-5, 2009.
Article in English | MEDLINE | ID: mdl-19480263

ABSTRACT

OBJECTIVE: To present an extremely rare case of a primary carcinoid tumor arising in a mature cystic teratoma of the ovary. Malignant transformation of mature cystic teratoma is an uncommon complication occuring in approximately 1-3% of patients with mature cystic teratoma. CLINICAL PRESENTATION AND INTERVENTION: A 54-year-old woman presented with abdominal swelling and abnormal uterine bleeding. Physical examination revealed a smooth, non-painful, 8-9 cm diameter mass in the right anterior pelvis which was diagnosed histologically as carcinoid tumor arising in a mature cystic teratoma. The patient underwent a total abdominal hysterectomy with bilateral salpingo-oophorectomy and was scheduled for surveillance CT of the abdomen and pelvis at 3-monthly intervals. CONCLUSION: This case adds to the rare reports in the literature of a carcinoid of low malignant potential occurring in a mature cystic teratoma. The treatment for early-stage ovarian carcinoid tumors confined to one ovary is surgery alone and excellent outcomes can be expected in these cases.


Subject(s)
Carcinoid Tumor/pathology , Neoplasms, Multiple Primary/pathology , Ovarian Neoplasms/pathology , Female , Humans , Middle Aged , Teratoma
5.
Invest New Drugs ; 26(6): 567-72, 2008 Dec.
Article in English | MEDLINE | ID: mdl-18762864

ABSTRACT

In order to investigate the effect of kefir consumption on mucositis induced by 5-FU based chemotherapy (CT), we monitored the systemic immune response by measurement of the serum proinflammatory cytokine levels and we evaluated the anti-microbial effect of kefir with an agar diffusion method. Forty patients with colorectal cancer were included in this randomized prospective study. On the first 5 days of each CT cycle, the study group received oral lavage with kefir and then swallowed 250 ml of kefir while control group received oral lavage with 0.09% NaCl twice a day. Before and after every cycle of CT, the oral mucosa was assessed. Serum proinflammatory cytokine levels were evaluated before the initiation and after the third and the sixth cycle. Kefir was administered in 99 out of 205 courses. Mucositis developed in 27.3% of the courses given with kefir administration and in 21.7% of the courses given with 0.9% NaCl oral rinses. The difference between the two groups was not statistically significant (p > 0.05). When we compared the serum proinflammatory cytokine levels of the two groups at the baseline and following the third and the sixth cycles, we again found no statistically significant difference (p > 0.05). Kefir consumption at the mentioned doses made no statistically significant effect on serum proinflammatory cytokine levels and on the incidence of mucositis development in cancer patients. Under in vitro conditions, kefir inhibits only Staphylococcus epidermidis.


Subject(s)
Antimetabolites, Antineoplastic/adverse effects , Cultured Milk Products , Fluorouracil/adverse effects , Stomatitis/prevention & control , Administration, Oral , Adult , Aged , Colorectal Neoplasms/drug therapy , Cytokines/blood , Cytokines/drug effects , Female , Humans , Inflammation Mediators/blood , Male , Middle Aged , Mouth Mucosa/drug effects , Mouth Mucosa/pathology , Prospective Studies , Stomatitis/chemically induced , Young Adult
6.
Ann Oncol ; 19(4): 669-74, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18006896

ABSTRACT

BACKGROUND: Triple-negative breast cancer is estimated to account for 15%-20% of all patients with breast cancer and is considered as a prognostically unfavorable subset. The aim of this study is to evaluate the prognostic impact of various molecular factors in patients with triple-negative breast cancer. PATIENTS AND METHODS: Tumor specimens from 109 patients with receptor-negative (estrogen receptor and progesterone receptor) breast cancer were analyzed for mitogen-activated protein kinase (MAPK), epidermal growth factor receptor (EGFR) and phosphoinositol-3-kinase (PI3K) expression by immunohistochemistry. The prognostic significance of these molecular factors, in addition to various prognostic variables, was investigated. RESULTS: Fifteen (13.8%), 38 (34.9%) and 33 patients (30.3%) had positive staining for EGFR, MAPK and PI3K, respectively. MAPK was associated with anthracycline resistance (P = 0.008) and lower MAPK score was significantly associated with shorter disease-free survival (P = 0.029). Survival following relapse was significantly worse for those with a higher MAPK score (P = 0.03). CONCLUSION: MAPK is a significant prognostic and predictive factor in patients with triple-negative breast cancer. Furthermore, the level of staining among those with a positive MAPK expression may play a prognostic role at different stages of relapse. Further translational research is required to elucidate molecular mechanisms of tumor proliferation in this subset of patients.


Subject(s)
Anthracyclines/pharmacology , Antibiotics, Antineoplastic/pharmacology , Biomarkers, Tumor/analysis , Breast Neoplasms/enzymology , Drug Resistance, Neoplasm , Mitogen-Activated Protein Kinases/analysis , Neoplasm Recurrence, Local/enzymology , Adult , Aged , Anthracyclines/therapeutic use , Antibiotics, Antineoplastic/therapeutic use , Breast Neoplasms/chemistry , ErbB Receptors/analysis , Female , Gene Expression Regulation, Enzymologic , Gene Expression Regulation, Neoplastic , Humans , Immunohistochemistry , Middle Aged , Neoplasm Recurrence, Local/chemistry , Odds Ratio , Phosphatidylinositol 3-Kinases/analysis , Prognosis , Proportional Hazards Models , Risk Assessment , Risk Factors , Up-Regulation
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