Preoperative diagnosis of medullary thyroid carcinoma by RT-PCR using RNA extracted from leftover cells within a needle used for fine needle aspiration biopsy.

Fine needle aspiration Biopsy (FNAB) is commonly used to diagnose thyroid tumors. In some clinical situations, however, accurate diagnosis requires a more objective method than cytological examination alone. Medullary thyroid carcinomas (MTC) derive from C cells in the thyroid and express some specific messenger RNAs (mRNA), such as those transcribed from the RET proto-oncogene, the calcitonin gene, and the gene for carcinoembryonic antigen (CEA), which usually do not exist in normal thyroid follicular cells or thyroid tumors of follicular epithelial descent. Recently, we established a new method for the molecular diagnosis of thyroid tumors without additional invasion to the patient by extracting RNA for RT-PCR from the leftover cells inside the needles used for fine needle aspiration biopsy (Aspiration Biopsy-Reverse Transcription-Polymerase Chain Reaction, ABRP). By applying the ABRP method to the detection of RET, calcitonin, and CEA mRNAs, an accurate molecular-based diagnosis for MTC maybe established as an adjunct to cytological diagnosis. In this study, 35 aspirates were obtained at the time of surgery from thyroid tumors, including 11 MTCs. The expression of these mRNAs in the leftover cells inside the needles used for the aspiration was then examined. Transcripts from all three genes were detected in the samples from all 11 MTCs, but none of these mRNAs were detected in the other tumors or normal thyroid tissues. Furthermore, MTC was preoperatively diagnosed in three patients by ABRP detection of these mRNAs, and these diagnoses were confirmed by subsequent cytological and histopathological analyses. Thus RT-PCR detection of RET, calcitonin, and CEA mRNAs in FNABs may be an efficient molecular adjunct for diagnosing MTC.

[1]  A. Miyauchi,et al.  Accurate and objective preoperative diagnosis of thyroid papillary carcinomas by reverse transcription-PCR detection of oncofetal fibronectin messenger RNA in fine-needle aspiration biopsies. , 1998, Cancer research.

[2]  A. Miyauchi,et al.  Restricted expression of oncofetal fibronectin mRNA in thyroid papillary and anaplastic carcinoma: an in situ hybridization study. , 1998, British Journal of Cancer.

[3]  L. Mulligan,et al.  Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation. , 1997, The Journal of clinical endocrinology and metabolism.

[4]  B. Ponder,et al.  Germline mutation of RET codon 883 in two cases of de novo MEN 2B , 1997, Oncogene.

[5]  T. Takano,et al.  Detection of CD44 variants in fine needle aspiration biopsies of thyroid tumor by RT-PCR. , 1997, Journal of experimental & clinical cancer research : CR.

[6]  F. Matsuzuka,et al.  Rapid detection of specific messenger RNAs in thyroid carcinomas by reverse transcription-PCR with degenerate primers: specific expression of oncofetal fibronectin messenger RNA in papillary carcinoma. , 1997, Cancer research.

[7]  T. Takano,et al.  Quantitative analysis of rat thyroglobulin messenger RNA in FRTL-5 cells by competitive polymerase chain reaction with human thyroglobulin messenger RNA. , 1997, Endocrine research.

[8]  C Eng,et al.  The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. , 1996, JAMA.

[9]  A. Miyauchi,et al.  Thyroid Cancer Detected by Ultrasound-Guided Fine-Needle Aspiration Biopsy , 1996, World Journal of Surgery.

[10]  M. Weiss,et al.  Preoperative diagnosis of thyroid papillary carcinoma by reverse transcriptase polymerase chain reaction of the MUC1 gene , 1996, International journal of cancer.

[11]  H. Cramer,et al.  Fine needle aspiration of medullary carcinoma of the thyroid. Cytomorphology, immunocytochemistry and electron microscopy. , 1995, Acta cytologica.

[12]  M. Schlumberger,et al.  RET mutations in exons 13 and 14 of FMTC patients. , 1995, Oncogene.

[13]  A. Miyauchi,et al.  Accurate and simple method of diagnosing thyroid nodules the modified technique of ultrasound-guided fine needle aspiration biopsy. , 1995, Thyroid : official journal of the American Thyroid Association.

[14]  B. Ponder,et al.  A novel point mutation in the tyrosine kinase domain of the RET proto-oncogene in sporadic medullary thyroid carcinoma and in a family with FMTC. , 1995, Oncogene.

[15]  J. Hamburger Diagnosis of thyroid nodules by fine needle biopsy: use and abuse. , 1994, The Journal of clinical endocrinology and metabolism.

[16]  A. Porcellini,et al.  Novel mutations of thyrotropin receptor gene in thyroid hyperfunctioning adenomas. Rapid identification by fine needle aspiration biopsy. , 1994, The Journal of clinical endocrinology and metabolism.

[17]  A. Pinchera,et al.  Expression of thyrotropin receptor (TSH-R), thyroglobulin, thyroperoxidase, and calcitonin messenger ribonucleic acids in thyroid carcinomas: evidence of TSH-R gene transcript in medullary histotype. , 1994, The Journal of clinical endocrinology and metabolism.

[18]  P. Goodfellow,et al.  Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[19]  C. Healey,et al.  Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours. , 1994, Human molecular genetics.

[20]  R. Hofstra,et al.  A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma , 1994, Nature.

[21]  D. Clayton,et al.  Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC , 1994, Nature Genetics.

[22]  B. Ponder,et al.  Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A , 1993, Nature.

[23]  A. Pinchera,et al.  Medullary thyroid cancer. An immunohistochemical and humoral study using six separate antigens. , 1991, American journal of clinical pathology.

[24]  M. Santoro,et al.  The ret proto-oncogene is consistently expressed in human pheochromocytomas and thyroid medullary carcinomas. , 1990, Oncogene.

[25]  A. Grauer,et al.  Changing concepts in the management of hereditary and sporadic medullary thyroid carcinoma. , 1990, Endocrinology and metabolism clinics of North America.

[26]  I. Hay Papillary thyroid carcinoma. , 1990, Endocrinology and metabolism clinics of North America.

[27]  T. Iwamoto,et al.  Cloning and expression of the ret proto-oncogene encoding a tyrosine kinase with two potential transmembrane domains. , 1988, Oncogene.

[28]  S. Goebel,et al.  Carcinoembryonic antigen family: characterization of cDNAs coding for NCA and CEA and suggestion of nonrandom sequence variation in their conserved loop-domains. , 1988, Genomics.

[29]  Y. Malthiéry,et al.  Primary structure of human thyroglobulin deduced from the sequence of its 8448-base complementary DNA. , 1987, European journal of biochemistry.

[30]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[31]  O. Beahrs,et al.  Medullary carcinoma of the thyroid gland , 1975, Cancer.

[32]  T. Martin,et al.  Identification of calcitonin and calcitonin gene-related peptide messenger ribonucleic acid in medullary thyroid carcinomas by hybridization histochemistry. , 1986, The Journal of clinical endocrinology and metabolism.

[33]  S. Foord,et al.  Expression and function of the human calcitonin/alpha-CGRP gene in health and disease. , 1986, Biochemical Society Symposium.

[34]  P. Arcari,et al.  The complete sequence of a full length cDNA for human liver glyceraldehyde-3-phosphate dehydrogenase: evidence for multiple mRNA species. , 1984, Nucleic acids research.

[35]  R. Lloyd,et al.  Calcitonin, carcinoembryonic antigen and neuron‐specific enolase in medullary thyroid carcinoma. An immunohistochemical study , 1983, Cancer.

[36]  B. Cady,et al.  Nonfamilial medullary thyroid carcinoma. , 1980, American journal of surgery.