2401. [Biology of bronchial cancer. Molecular epidemiology].2402. [New target tissues for aldosterone].2403. [Ovarian mucinous tumor of gastric and intestinal type associated with Peutz-Jeghers syndrome: in situ hybridization study of apomucin gene transcripts].
作者: A Wacrenier.;F Boman.;M O Farine.;M Durand-Reville.;M P Buisine.;N Porchet.;J P Aubert.;D Querleu.;B Gosselin.
来源: Ann Pathol. 1998年18卷6期497-501页
Occurrence of mucinous tumors is favored by Peutz-Jeghers syndrome (PJS). A case of bilateral ovarian mucinous tumor associated with ovarian mature teratoma occurring in a 22-year-old woman with PJS was reported. Tumor cells included 5 cell types: tall columnar mucinous pale cells with neutral mucins; goblet cells with acidic nonsulfated mucins; non mucinous columnar cells; mucinous cuboidal cells lining small glands; endocrine cells. Expression of the MUC2, MUC3, MUC5AC and MUC6 genes was demonstrated by in situ hybridization according to cell type. Some atypia and numerous mitotic figures were observed in basal glands. Diagnosis was ovarian borderline mucinous tumor with gastric and intestinal phenotype associated with PJS.
2404. [A balance of clinical trials in gene therapy].2406. [Cytogenetics of malignant hemopathies: update].2407. [Update on genetic markers of cancer].2408. [Bright note on the molecular mechanisms of oncogenic transformation].2409. [Protective immunity against lymphoma and myeloma in mice with an anti-idiotypic DNA base vaccine].2410. [P27Kip1 is certainly a suppressor gene but with a dose effect].2411. [Smad3-/- mice: a murine model for the study of human colorectal cancers?].2412. [XPD (ERCC2) (Xeroderma pigmentosum, group D). Reparation gene].
来源: Bull Cancer. 1998年85卷12期987-8页
2413. [Ret (REarranged during Transfection). Oncogene].
来源: Bull Cancer. 1998年85卷12期985-6页
2415. [The role of APC in colonic cancerogenesis: zeroing in on Myc].
The APC gene is mutated both in familial adenomatous polyposis (FAP) and sporadic colorectal cancers. It had been previously shown that the APC gene product interacts with beta-catenin, a key element in the Wnt-1 signaling pathway. This pathway is initiated by the growth factor Wnt-1 and ends up in the nucleus where it activates transcription factors of the Lef/Tcf family although the targets of the latter were still unknown. This has just been accomplished by the identification of the c-MYC oncogene as the relevant target of the Wnt-1/APC pathway in the development of human colorectal cancers. Indeed, under appropriate conditions (presence of growth factors, for example), c-MYC is an essential determinant of cell proliferation.
2416. [Sixth congress of the European Genetic Therapy Group].2417. [Epithelial ovarian cancers (advanced stage)].
Ovarian carcinomas are known to have a poor prognosis, not only because their diagnosis is often made in late time, but the risk of recurrence after initial treatment is high. This overview was made to explain the different approaches while dealing with a patient with an ovarian carcinoma. A particular interest went to the familial history of ovarian cancer, concerning a very short population, as shown in the recent data. Prognostic factors, the way of diagnosis, and the histologic classification were also explained in detail. Ovarian cancer is more often found out at an advanced stage of the disease, that's the reason why the treatment of epithelial ovarian cancer was extensively studied, with the recent approaches of the new drugs; for instance, the use of combinations with taxoides in the first part of treatment, or a numerous of other agents, particularly at the time of the recurrence, like the camptothecines, the gemcitabine, or the new derivatives of platinum. The management of the patient after initial treatment (follow up, maintenance therapy) were also included in this overview. As for the "borderline" tumors, a peculiar chapter was devoted to them.
2418. Specific features of a group of multifactorial diseases: the genetics of tumors.2419. A mouse model for learning and memory defects associated with neurofibromatosis type I.2420. Mutations in XPD helicase prevent its interaction and regulation by p44, another subunit of TFIIH, resulting in Xeroderma pigmentosum (XP) and trichothiodystrophy (TTD) phenotypes. |