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 Ras Gene02:38

The Ras Gene

7.5K
The Ras-gene-encoded proteins are regulators of signaling pathways controlling cell proliferation, differentiation, or cell survival. The Ras-gene family in humans constitutes three primary members—the HRas, NRas, and KRas. These genes code for four functionally distinct yet closely related proteins—the HRas, NRas, KRas4A, and KRas4B. The involvement of mutant Ras genes in human cancer was first discovered in 1982 and is among the most common causes of human tumorigenesis.
Ras is a...
7.5K
Abnormal Proliferation02:23

Abnormal Proliferation

5.4K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
5.4K
The Ras Gene02:38

The Ras Gene

2.5K
2.5K
Small GTPases - Ras and Rho01:24

Small GTPases - Ras and Rho

5.7K
Ras and Rho are small monomeric GTPases that act downstream of receptor tyrosine kinase (RTK) and regulate various cellular processes. These GTPases switch between active and inactive states by binding to guanine nucleotides.
Three regulatory proteins control their activity:
5.7K
Tumor Progression02:07

Tumor Progression

7.9K
Tumor progression is a phenomenon where the pre-formed tumor acquires successive mutations to become clinically more aggressive and malignant. In the 1950s, Foulds first described the stepwise progression of cancer cells through successive stages.
Colon cancer is one of the best-documented examples of tumor progression. Early mutation in the APC gene in colon cells causes a small growth on the colon wall called a polyp. With time, this polyp grows into a benign, pre-cancerous tumor. Further...
7.9K
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

5.1K
The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
5.1K

You might also read

Related Articles

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

Sort by
Same author

Ketogenic and Low-Carbohydrate Diets in Prostate Cancer: Metabolic Rationale, Preclinical Evidence, and Preliminary Clinical Data.

Journal of clinical medicine·2026
Same author

Gastric cancer, what's new from International Gastric Cancer Congress (IGCC) in Amsterdam: a scientific report from Salerno 2025 conference.

Ecancermedicalscience·2026
Same author

Somatic genomic profiling reveals clinically relevant heterogeneity in <i>RAS</i>-mutant sporadic medullary thyroid carcinoma.

Journal of clinical & translational endocrinology·2026
Same author

Diabetes and cancer: glucose control impact on survival and tumor outcomes.

Reviews in endocrine & metabolic disorders·2026
Same author

Clinical Impact of Rare Subtypes of Parathyroid Adenoma: A Systematic Review.

Journal of personalized medicine·2026
Same author

Anti-Ma2 Paraneoplastic Encephalitis and Testicular Cancer: When the Hypothalamus Whispers-A Case Report and Systematic Review with Emphasis on Hypothalamic-Endocrine Dysfunction.

Medical sciences (Basel, Switzerland)·2026

Related Experiment Video

Updated: Apr 5, 2026

Establishment and Characterization of Patient-Derived Xenograft Models of Anaplastic Thyroid Carcinoma and Head and Neck Squamous Cell Carcinoma
06:08

Establishment and Characterization of Patient-Derived Xenograft Models of Anaplastic Thyroid Carcinoma and Head and Neck Squamous Cell Carcinoma

Published on: June 2, 2023

2.6K

Benign thyroid nodules with RAS mutation grow faster.

Alessandro Puzziello1, Anna Guerra1, Alessia Murino1

  • 1Department of Medicine and Surgery, University of Salerno, Baronissi, Italy.

Clinical Endocrinology
|August 12, 2015
PubMed
Summary

RAS mutations in benign thyroid nodules are linked to faster growth. Identifying these mutations can help predict nodule size changes and guide timely surgical decisions for patients.

More Related Videos

An Orthotopic Mouse Model of Anaplastic Thyroid Carcinoma
07:01

An Orthotopic Mouse Model of Anaplastic Thyroid Carcinoma

Published on: April 17, 2013

21.8K
Spontaneous Murine Model of Anaplastic Thyroid Cancer
05:39

Spontaneous Murine Model of Anaplastic Thyroid Cancer

Published on: February 3, 2023

2.4K

Related Experiment Videos

Last Updated: Apr 5, 2026

Establishment and Characterization of Patient-Derived Xenograft Models of Anaplastic Thyroid Carcinoma and Head and Neck Squamous Cell Carcinoma
06:08

Establishment and Characterization of Patient-Derived Xenograft Models of Anaplastic Thyroid Carcinoma and Head and Neck Squamous Cell Carcinoma

Published on: June 2, 2023

2.6K
An Orthotopic Mouse Model of Anaplastic Thyroid Carcinoma
07:01

An Orthotopic Mouse Model of Anaplastic Thyroid Carcinoma

Published on: April 17, 2013

21.8K
Spontaneous Murine Model of Anaplastic Thyroid Cancer
05:39

Spontaneous Murine Model of Anaplastic Thyroid Cancer

Published on: February 3, 2023

2.4K

Area of Science:

  • Endocrinology
  • Molecular Biology
  • Oncology

Background:

  • Benign thyroid nodules require monitoring for size changes that may necessitate intervention.
  • Predicting benign thyroid nodule growth is challenging due to a lack of specific growth parameters.
  • RAS mutations are found in thyroid adenomas and hyperplastic benign nodules.

Purpose of the Study:

  • To determine if volume changes in benign thyroid nodules correlate with the presence of RAS mutations.

Main Methods:

  • Analyzed genomic DNA from 78 benign thyroid nodules via fine-needle aspiration for NRAS(61) and KRAS(13) mutations.
  • Assessed ultrasonographic features and nodule volumes at baseline.
  • Evaluated nodule volume changes over a mean 25-month follow-up period based on RAS mutation status.

Main Results:

  • RAS mutations were detected in 30.8% of benign thyroid nodules (24/78).
  • RAS mutations were associated with larger baseline nodule size (P = 0.017) but not ultrasonographic features.
  • Nodules with RAS mutations exhibited significantly faster annual growth (27.6%) compared to wild-type nodules (1.0%) (P < 0.001).

Conclusions:

  • Benign thyroid nodules with RAS mutations demonstrate accelerated growth compared to those without.
  • Detecting RAS mutations in benign thyroid nodules can aid clinicians in optimizing surgical management timing.