## Abstract ## BACKGROUND hMLH1, the human MutL homologue, has been linked to microsatellite instability (MSI) in gastrointestinal tumors. However, to the authors' knowledge, the role of hMLH1, the other mismatch repair genes (MMR), and MSI in ovarian carcinoma has not been well defined. The purpo
Mismatch repair gene expression defects contribute to microsatellite instability in ovarian carcinoma
โ Scribed by Tuya Pal; Rebecca Sutphen; Thomas Sellers
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 69 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
โฆ Synopsis
Cancer-Related Fatigue: Evolving Concepts in Evaluation and Treatment
I n their otherwise excellent review of cancer-related fatigue, Stasi et al. 1 failed to discuss opioid-induced androgen deficiency (OPIAD), an extremely common and easily identified cause of fatigue in men with malignant disease.
Testosterone deficiency develops within a few hours after the ingestion of oral sustained-action opioids in the majority of men, and this deficiency is continuously present in most men who receive these agents several times daily, 2 as well as in most men who receive intrathecally 3 or transdermally administered 4 opioids. OPIAD, like other forms of hypogonadism, characteristically contributes to muscle wasting, anemia, osteoporosis, and depression in men with cancer, and it also often causes night sweats and other vasomotor events. A similar phenomenon is observed among women who receive opioids, as these women commonly develop low gonadotropin and sex hormone levels.
Intramuscular or transdermal testosterone therapy frequently results in gratifying improvements for individuals with OPIAD. In my experience, OPIAD-associated depression is unlikely to respond to antidepressant medications in the absence of testosterone replacement.
๐ SIMILAR VOLUMES
Our previous studies of lung cancer in chromate-exposed workers (chromate lung cancer) have revealed that the frequency of replication error (RER) in chromate lung cancer is very high. We examined whether the RER phenotype of chromate lung cancer is due to an abnormality of DNA mismatch repair prote
## Background: Several convincing studies have shown that the hmsh2 gene plays major roles in mismatch repair by recognizing mismatched bases and preventing mutations during dna replication. loss of this function may result in the accumulation of dna replication errors or even the mutator phenotype