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 Concept Videos

The Nucleolus02:55

The Nucleolus

10.8K
The nucleolus is the most prominent substructure of the nucleus. When it was first discovered, it was considered to be an isolated organelle that forms fibrils and granules. In 1931, the relationship between the nucleolus and chromosomes was first described by Heitz. He observed that the appearance and size of nucleolus varies depending on the stage of the cell cycle. He also noticed constricted regions on different chromosomes clustered together at definite cell cycle stages. These regions,...
10.8K
Synthesis and Regulation of Thyroid Hormones01:20

Synthesis and Regulation of Thyroid Hormones

9.4K
Low blood levels of the thyroid hormones — triiodothyronine (T3) and thyroxine (T4) — signal the hypothalamus to release the thyrotropin-releasing hormone (TRH). TRH then reaches the pituitary gland and stimulates the release of thyroid-stimulating hormone(TSH) into the bloodstream.
Upon reaching the thyroid gland, TSH stimulates the follicular cells' active uptake of iodide ions from the blood. The ions diffuse to the apical surface of the cells and are oxidized to iodine. The...
9.4K
RNA Splicing01:32

RNA Splicing

61.8K
Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
61.8K
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

10.2K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
10.2K

You might also read

Related Articles

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

Sort by
Same author

The Italian Unitary Society of Colon-Proctology (SIUCP: Società Italiana Unitaria di Colonproctologia) guidelines for the management of obstructed and ineffective defecation syndrome.

Annals of coloproctology·2026
Same author

Chorus line in oral squamous cell carcinoma: How stromal and immune players orchestrate tumor progression (Review).

International journal of molecular medicine·2026
Same author

Editorial: Thyroid and parathyroid surgery: new and emerging concepts.

Frontiers in surgery·2025
Same author

Transverse perineal support improves long-term outcomes in patients undergoing stapled transanal rectal resection for obstructed defecation syndrome: a multicenter observational case-control study.

Annals of coloproctology·2025
Same author

Isolation of endothelial progenitor cells from human adipose tissue.

International journal of obesity (2005)·2025
Same author

Oral Undifferentiated Pleomorphic Sarcoma: A Novel <i>SPECC1L::TERT</i> Gene Fusion and a Comprehensive Literature Review.

Genes·2025

Related Experiment Video

Updated: Apr 13, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
07:02

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice

Published on: August 23, 2019

7.9K

Clusterin transcript variants expression in thyroid tumor: a potential marker of malignancy?

Paolo Fuzio1, Anna Napoli2, Anna Ciampolillo3

  • 1Institute of Biomedical Technologies, National Research Council (CNR), Via G. Amendola, 122/D, 70126, Bari, Italy. paolo.fuzio@ba.itb.cnr.it.

BMC Cancer
|May 3, 2015
PubMed
Summary

Clusterin (CLU) transcript variants show altered expression in thyroid cancer, with CLU2 increasing while CLU1 decreases. This CLU2:CLU1 ratio shift may help diagnose indeterminate thyroid nodules.

More Related Videos

Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers
03:37

Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers

Published on: March 1, 2024

1.5K
An Ex vivo Culture System to Study Thyroid Development
08:33

An Ex vivo Culture System to Study Thyroid Development

Published on: June 6, 2014

12.2K

Related Experiment Videos

Last Updated: Apr 13, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
07:02

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice

Published on: August 23, 2019

7.9K
Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers
03:37

Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers

Published on: March 1, 2024

1.5K
An Ex vivo Culture System to Study Thyroid Development
08:33

An Ex vivo Culture System to Study Thyroid Development

Published on: June 6, 2014

12.2K

Area of Science:

  • Molecular biology
  • Oncology
  • Biomarker research

Background:

  • Clusterin (CLU) is a multifunctional protein involved in cell proliferation and death.
  • CLU transcript variants play a critical role in neoplastic transformation.

Purpose of the Study:

  • To investigate the regulation of CLU transcript variants expression.
  • To assess the potential of CLU transcript variants as biomarkers for thyroid nodules.

Main Methods:

  • In vivo model system using neoplastic tissues and fine needle aspiration biopsy (FNAB) samples.
  • Immunohistochemical analyses for CLU expression.
  • Quantitative polymerase chain reaction (qPCR) to analyze CLU transcript variants (CLU1 and CLU2).

Main Results:

  • Overall CLU up-regulation observed in papillary carcinoma.
  • Specific increase in CLU2 transcript and decrease in CLU1 transcript in papillary carcinomas.
  • Increased CLU2 transcript levels in patients with histologically confirmed thyroid cancer (TIR 3).

Conclusions:

  • A specific alteration in the CLU2:CLU1 ratio favoring CLU2 was identified.
  • This finding provides evidence for CLU transcript variants as potential biomarkers.
  • CLU variants could aid in the accurate assessment of indeterminate thyroid nodules.