Ultrastructure, steroidogenic potential, and energy metabolism of the Snell adrenocortical carcinoma 494. A comparison with normal adrenocortical tissue
- PMID: 4366105
- PMCID: PMC2109177
- DOI: 10.1083/jcb.62.1.152
Ultrastructure, steroidogenic potential, and energy metabolism of the Snell adrenocortical carcinoma 494. A comparison with normal adrenocortical tissue
Abstract
Electron microscope studies were carried out with the adrenocortical carcinoma 494 and normal adrenal cortex tissue. The mitochondria of the tumor cells showed marked differences when compared with mitochondria from fasciculata cells of the normal adrenal cortex. These differences were primarily related to mitochondrial number and crista structure. Corticosterone production in isolated tumor cells was extremely low and neither ACTH nor dibutyryl cyclic AMP had any stimulatory effect. Normal adrenal cells showed at least a tenfold increase under identical conditions. In the presence of corticosteroid precursors the amount of corticosterone produced by the tumor cells was much less than that produced by normal cells. The results indicate a reduced capacity for 11beta-hydroxylation in the tumor mitochondria and a possible reduced capacity for biosynthetic steps before the 11beta-hydroxylation reaction. Glycolysis in isolated tumor cells was also lower than in normal cells. Isolated tumor mitochondria oxidized succinate normally with a good degree of coupling with phosphorylation. However, unlike normal adrenal mitochondria, the tumor mitochondria showed little or no oxygen uptake with other Krebs cycle substrates. These data suggest that the tumor mitochondria may be lacking in the flavoprotein dehydrogenases responsible for the oxidation of NADH and NADPH, although other components of the respiratory chain may be intact.
Similar articles
-
Studies on respiration and 11 beta-hydroxylation of deoxycorticosterone in mitochondria and intact cells isolated from the Snell adrenocortical carcinoma 494.Cancer Res. 1974 Oct;34(10):2711-9. Cancer Res. 1974. PMID: 4153485 No abstract available.
-
Abnormal regulation of adenosine 3',5'-monophosphate and corticosterone formation in an adrenocortical carcinoma.J Clin Invest. 1969 Sep;48(9):1733-9. doi: 10.1172/JCI106139. J Clin Invest. 1969. PMID: 4390412 Free PMC article.
-
Characteristics of the response of human adrenocortical cells to ACTH.Mol Cell Endocrinol. 1976 Aug-Sep;5(3-4):255-67. doi: 10.1016/0303-7207(76)90088-5. Mol Cell Endocrinol. 1976. PMID: 182579
-
Inhibition of replication of normal adrenocortical cells in culture by adrenocorticotropin.Proc Natl Acad Sci U S A. 1975 Jan;72(1):113-7. doi: 10.1073/pnas.72.1.113. Proc Natl Acad Sci U S A. 1975. PMID: 164010 Free PMC article.
-
Sources of reducing equivalents for cytochrome P-450 mitochondrial steroid hydroxylations in rat adrenal cortex cells.J Steroid Biochem. 1975 Mar-Apr;6(3-4):411-7. doi: 10.1016/0022-4731(75)90165-x. J Steroid Biochem. 1975. PMID: 1102797 Review. No abstract available.
Cited by
-
Altered expression of the IGF2‑H19 locus and mitochondrial respiratory complexes in adrenocortical carcinoma.Int J Oncol. 2022 Nov;61(5):140. doi: 10.3892/ijo.2022.5430. Epub 2022 Sep 28. Int J Oncol. 2022. PMID: 36169175 Free PMC article.
-
Lanthanum: inhibition of ACTH-stimulated cyclic AMP and corticosterone synthesis in isolated rat adrenocortical cells.J Cell Biol. 1976 Jan;68(1):142-53. doi: 10.1083/jcb.68.1.142. J Cell Biol. 1976. PMID: 173723 Free PMC article.