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Related Concept Videos

Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
Rous Sarcoma Virus (RSV) and Cancer01:03

Rous Sarcoma Virus (RSV) and Cancer

Rous Sarcoma virus or RSV was discovered by F. Peyton Rous in the year 1911 as a filterable transmissible agent that could cause tumors in chickens. He won a Nobel Prize for this discovery in 1966. His experiments clearly demonstrated that some cancers could be caused by infectious agents and led to the discovery of many more cancer-causing viruses in animals as well as humans.
RSV is a retrovirus that contains two copies of a plus-strand  RNA genome. Its genome consists of four main open...
Non-LTR Retrotransposons03:18

Non-LTR Retrotransposons

As the name suggests, non-LTR retrotransposons lack the long terminal repeats characteristic of the LTR retrotransposons. Additionally, both LTR and non-LTR retrotransposons use distinct mechanisms of mobilization. Non-LTR retrotransposons are further divided into two classes - Long interspersed nuclear elements (LINEs) and short interspersed nuclear elements (SINEs), both of which occur abundantly in most mammals, including humans. Some of the active non-LTR retrotransposons in humans are L1...
Metastasis02:30

Metastasis

Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
Tumor Progression02:07

Tumor Progression

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...
Post-translational Translocation of Proteins to the RER01:27

Post-translational Translocation of Proteins to the RER

A sizable fraction of proteins destined for ER are first synthesized in the cell cytosol and then transported across the ER membrane–a process called post-translational translocation. Similar to cotranslationally translocated proteins, these proteins also use the Sec translocon complex to enter the ER lumen.
Targeting proteins to the ER
Hsp40 and Hsp70 chaperone molecules bind the translated proteins in the cytosol to prevent their folding. The chaperone binding helps to keep the signal...

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Related Experiment Video

Updated: Jun 21, 2026

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
11:42

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells

Published on: April 7, 2017

Translocation-related sarcomas.

Fredrik Mertens1, Cristina R Antonescu, Peter Hohenberger

  • 1Department of Clinical Genetics, Lund University Hospital, Lund, Sweden.

Seminars in Oncology
|August 12, 2009
PubMed
Summary
This summary is machine-generated.

Translocation-associated sarcomas, though uncommon, offer unique biological insights similar to GIST. Understanding their mechanisms is key for developing targeted therapies and improving patient prognosis.

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Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Sarcomas are a diverse group of cancers.
  • Chromosomal translocations are found in approximately 25% of sarcoma diagnoses.
  • Specific mutations in gastrointestinal stromal tumors (GIST) like KIT or PDGFRA offer therapeutic targets.

Purpose of the Study:

  • To review the biology of translocation-associated sarcomas.
  • To discuss the clinical impact of these specific sarcoma subtypes.
  • To highlight recent clinical findings relevant to patient treatment.

Main Methods:

  • Literature review of biological mechanisms.
  • Analysis of clinical findings and patient outcomes.
  • Synthesis of current research on translocation-associated sarcomas.

Main Results:

  • Translocation-associated sarcomas provide distinct biological insights.
  • These insights into specific mechanisms are beginning to be therapeutically exploited.
  • Recent clinical findings are impacting patient management.

Conclusions:

  • Translocation-associated sarcomas, while a minority, are crucial for understanding sarcoma biology.
  • Targeting specific translocation-driven mechanisms holds therapeutic potential.
  • Continued research into these sarcomas can lead to improved prognoses and treatments.