Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Molecular basis off hurthle cell papillary thyroid carcinoma.

C C Cheung1, S Ezzat, L Ramyar

  • 1Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, University of Toronto, Ontario, Canada.

The Journal of Clinical Endocrinology and Metabolism
|February 26, 2000
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Duplication of the portal vein and the implications for procedural planning.

Hong Kong medical journal = Xianggang yi xue za zhi·2025
Same author

Imaging with an inverse-designed 50 mm-diameter f/1 MWIR flat lens with enhanced field of view and depth of focus.

Optics letters·2024
Same author

Correction: CEACAM1 impedes thyroid cancer growth but promotes invasiveness: a putative mechanism for early metastases.

Oncogene·2023
Same author

Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory services.

European journal of medical genetics·2022
Same author

<i>Fermi</i> LARGE AREA TELESCOPE OBSERVATIONS OF BLAZAR 3C 279 OCCULTATIONS BY THE SUN.

The Astrophysical journal·2021
Same author

A primer on the genetics of medullary thyroid cancer.

Current oncology (Toronto, Ont.)·2020

A subset of Hurthle cell tumors (HCTs) show features of papillary thyroid carcinoma (PTC) due to specific gene rearrangements. This finding supports classifying HCTs into adenomas, carcinomas, and PTC.

Area of Science:

  • Endocrinology
  • Oncology
  • Molecular Biology

Background:

  • Hurthle cell tumors (HCTs) are a distinct category of thyroid neoplasms.
  • Hurthle cell adenomas are benign, while Hurthle cell carcinomas are aggressive with poor prognosis.
  • Recent identification of Hurthle cell papillary thyroid carcinomas (PTCs) suggests underlying molecular events.

Purpose of the Study:

  • To investigate if a subset of HCTs represent PTC with specific molecular alterations.
  • To examine HCTs for ret/PTC gene rearrangements, which are unique to PTC.
  • To correlate molecular findings with clinical and histological features.

Main Methods:

  • Studied 50 HCTs for ret/PTC gene rearrangements.
  • Assessed papillary differentiation via light microscopy of nuclear features.

Related Experiment Videos

  • Utilized RT-PCR for ret/PTC gene transcripts and immunohistochemistry for ret protein expression.
  • Main Results:

    • Among 24 noninvasive tumors, 13 had ret/PTC transcripts, with 9 showing ret positivity.
    • Among 19 Hurthle cell carcinomas, 15 exhibited papillary features, ret/PTC transcripts, and ret positivity.
    • Tumors with ret/PTC rearrangements were more prone to lymph node metastasis than hematogenous spread.

    Conclusions:

    • A subset of HCTs display PTC features linked to specific ret/PTC gene rearrangements and oncogene expression.
    • These findings support the subclassification of HCTs into Hurthle cell adenomas, Hurthle cell carcinomas, and Hurthle cell PTC.
    • This molecular-based subclassification refines the understanding and management of thyroid neoplasms.