Growth Hormone Receptor Messenger Ribonucleic Acid in Normal and Pathologic Human Adrenocortical Tissues—An Analysis by Quantitative Polymerase Chain Reaction Technique1
GH receptor (GHR) has been reported to express in both normal rat and human adrenals. However, no study examined GHR expression in diseased human adrenal cortex. We quantitated, with RT-PCR, GHR messenger RNA (mRNA) in both normal and diseased human adrenal cortex with the following results: GHR mRN...
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Veröffentlicht in: | The journal of clinical endocrinology and metabolism 1997-08, Vol.82 (8), p.2671-2676 |
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Sprache: | eng |
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Zusammenfassung: | GH receptor (GHR) has been reported to express in both normal rat and
human adrenals. However, no study examined GHR expression in diseased
human adrenal cortex. We quantitated, with RT-PCR, GHR messenger RNA
(mRNA) in both normal and diseased human adrenal cortex with the
following results: GHR mRNA levels in four histologically normal, not
steroid-stimulated, control adrenal cortices was 1.5–11 ×
104 molecules/μg total RNA; in three diffusely
hyperplastic adrenals (DH): 6.7–17.7 × 104; in two
nonfunctioning tumors (NF): 0.84–1.9 × 104; in five
androgen-producing neoplasms (AP): 4.6–34 × 104; and
in five glucocorticoid-producing neoplasms (GP): 6.7–87 ×
104. GHR transcript levels among adrenal cortices, DH, NF,
AP, and GP reached statistically significant difference
(P < 0.03). The GP group exhibited higher GHR mRNA
levels than controls (P < 0.006). NF, as well as
GP and AP, tumors had less GHR mRNA than their histologically normal
adjacent cortex (P < 0.05). A positive correlation
between urinary cortisol and GHR messenger RNA (mRNA) levels from GP
and DH was observed (r = 0.93, P < 0.003).
Our data suggest that GHR is expressed in both normal and diseased
adrenal cortex and that GHR mRNA accumulation is less efficient in
adrenocortical neoplasm than their adjacent nonneoplastic cortex. GHR
expression in adrenal cortex provides an evidence of direct GH action
in this tissue. |
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ISSN: | 0021-972X 1945-7197 |
DOI: | 10.1210/jcem.82.8.4159 |