c-myc expression in the thyroid. I: Normal, adenomatous, and cancerous thyroid tissue

• Published in: Hormone and metabolic research. Supplement series Vol. 17; p. 63
• Main Authors: Burman, K D, Djuh, Y Y, LaRocca, R V, Nunes, M E, D'Avis, J C, Nicholson, D E, Wartofsky, L
• Format: Journal Article
• Language: English
• Published: Germany 1987
• Subjects: Adenoma - metabolism; Carcinoma - metabolism; Humans; Proto-Oncogene Proteins - biosynthesis; Proto-Oncogene Proteins - genetics; Proto-Oncogene Proteins c-myc; Proto-Oncogenes; RNA, Messenger - analysis; RNA, Neoplasm - analysis; Thyroid Gland - metabolism; Thyroid Neoplasms - metabolism
• ISSN: 0170-5903

Recent investigations have suggested that myc oncogene expression may be important in the development or progression of thyroid tumors. The purposes of the present study were to assess cellular (c)-myc expression in thyroid adenomas (n = 5), as well as in thyroid cancer (n = 4) and in normal thyrocytes (n = 7). Total RNA was prepared by extraction with guanididium thiocyanate and ultracentrifugation through a CsCl2 cushion. 30 micrograms total RNA was size fractionated on a 1% (w/v) agarose/formaldehyde gel and transferred to nylon membranes. These membranes were hybridized to a 32P-labelled third exon c-myc DNA. Following hybridization, blots were washed under high stringency and subjected to autoradiography; radioautographic bands were assessed visually or were quantitated by scanning densitometry. Nodular tissue had approximately the same degree of expression of the 2.4 Kb c-myc message as the surrounding normal tissue from the same gland (0.66 +/- 0.09 vs. 1.0 +/- 0.26, respectively); normal thyrocytes were capable in every instance of expressing the 2.4 Kb c-myc message. Thyroid cancer tissue expressed this message (0.91 +/- 0.17) but only at a level comparable to normal tissue. No other bands of hybridization were detected in any samples. We conclude that c-myc oncogene expression is comparable in normal thyrocytes and in thyroid nodules or thyroid cancer samples. These findings support a role for c-myc in both normal and neoplastic thyrocyte growth.