Cytophotometric measurements of nuclear DNA content in hepatocellular carcinomas
β Scribed by Sow-Hsong Kuo; Jin-Chuan Sheu; Ding-Shinn Chen; Juei-Low Sung; Chi-Chung Lin; Hey-Chi Hsu
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 330 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
β¦ Synopsis
Republic of China
The nuclear DNA contents of 64 hepatocellular carcinomas were measured on cytologic smears using a scanning microdensitometer at a wavelength of 660 nm. The cellular materials were aspirated under ultrasonographic guidance and stained with modified Feulgen method. The DNA modal values, which could be defined in 61 cases, ranged from 2.2 to 9.8 ploidy, with 46.3% (26/64) in hypertetraploidy. The hepatocellular carcinomas in patients with higher serum levels of a-fetoprotein contained more hyperploid cells. The DNA modal values did not correlate with the age, HBsAg status, tumor size and histological grading of hepatocellular carcinoma. The S-phase fraction values, which could be estimated on the DNA histograms in 43 cases (79.6%), ranged from 1 to 36 (mean f S.D. = 10.6 f 8.1). The Sphase fraction values were higher in high grade hepatocellular carcinomas (13.4 f 8.6) than low grade hepatocellular carcinomas (6.1 2 4.4), p < 0.01. The mean S-phase fraction values were also significantly higher in hepatocellular carcinomas with a-fetoprotein levels of more than 100 ng per ml than those of leas than 100 ng per ml (12.9 f 8.0 and 7.8 2 6.6, respectively). The S-phase fraction values also did not correlate with the age, HBsAg status and tumor size.
π SIMILAR VOLUMES
The prognostic significance of ploidy level was studied in prostatic carcinoma and compared with the prognostic significance of morphologic grade and clinical stage. A nonselected group of 145 patients was studied in whom prostatic carcinoma was diagnosed by fine-needle aspiration biopsy at the Karo
Cell division cycle (cdc) mutants of Schizosaccharomyces pombe are arrested at specific points in the cell cycle when grown at restrictive temperature. Flow cytometry of such cells reveals an anomalous increase in the DNA fluorescence signal, which represents a problem in experiments designed to det
Progression of breast neoplasia is characterized by a variety of causal and nonspecific molecular, karyotypic, and cellular level genetic alterations. These include allelic losses, chromosomal rearrangements, and aneusomies, as well as widely divergent clonal DNA content aberrations. Establishment o