Related Experiment Videos
Cytochemical markers of bladder carcinogenesis
The Histochemical Journal
|November 1, 1981
Summary
Altered enzyme localization, including alkaline phosphatase and 5'-nucleotidase, marks chemical transformation in rodent bladders. These enzyme changes, observed in tumors and cell cultures, indicate significant cellular alterations during carcinogenesis.
Area of Science:
- Biochemistry
- Cell Biology
- Oncology
Background:
- Chemical carcinogens induce significant alterations in cellular enzyme distribution.
- Understanding enzyme localization changes is crucial for identifying markers of chemical transformation in bladder tissues.
Purpose of the Study:
- To investigate the distribution of alkaline phosphatase, 5'-nucleotidase, and other enzymes in chemically induced rodent bladder tumors and cell cultures.
- To identify potential enzyme markers indicative of chemical transformation in bladder epithelium.
Main Methods:
- Enzyme cytochemistry and immunocytochemistry at light and electron microscope levels.
- In vivo induction of rat bladder tumors using methylnitrosourea.
- In vitro transformation of mouse bladder explants using dimethylbenz(a)anthracene.
- Organ culture of induced rat bladder tumors.
Main Results:
- Alkaline phosphatase showed abnormal intracellular localization in rat tumors, with heterogeneous plasma membrane distribution in organ culture.
- 5'-Nucleotidase exhibited abnormal intracellular localization in rat tumors and was lost after transformation in mouse cells.
- Transformed mouse bladder cells showed retained cAMP-phosphodiesterase as an ectoenzyme, induced Mg.ATPase, and a novel 'protein phosphatase', while losing ADPase.
Conclusions:
- Enzyme cytochemistry reveals distinct alterations in enzyme localization patterns associated with chemical transformation in rodent bladders.
- Changes in alkaline phosphatase and 5'-nucleotidase distribution serve as potential markers for bladder carcinogenesis.
- Specific enzyme induction and loss patterns differentiate normal from transformed bladder cells, offering insights into neoplastic progression.