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

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...
Bone Disorders01:29

Bone Disorders

Aging and its effect on bone remodeling is the most common cause of bone disorders. In young and healthy people, bone deposition and resorption happen at an equal rate to maintain optimal bone health.
Bone deposition is also affected by the levels of sex hormones like estrogen and testosterone that promote osteoblast activity and bone matrix synthesis. When the level of these hormones decreases due to aging, it causes a reduction in bone deposition. As a result, bone resorption by osteoclasts...

You might also read

Related Articles

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

Sort by
Same author

A bell that never rang: Accompanying a child through an endless class.

Palliative & supportive care·2026
Same author

<i>Candida albicans</i> RLM1 Diversity Regulates Cell Wall Composition and Virulence.

ACS infectious diseases·2026
Same author

Should we prioritize proton beam therapy before making a decision on orthotopic liver transplantation for unresectable hepatoblastoma?

The Turkish journal of pediatrics·2026
Same author

Comparative Effectiveness of Renin-Angiotensin System Inhibitors in Heart Failure With Nonreduced Ejection Fraction: A Multicenter Cohort Study.

Journal of cardiovascular pharmacology and therapeutics·2026
Same author

Genetic variation and mutational determinants of azole resistance in Candida albicans strains of oropharyngeal colonization in HIV patients and bloodstream infections.

Journal of biomedical science·2026
Same author

The relationship between urine output and time to methotrexate clearance in pediatric leukemia patients receiving high-dose methotrexate therapy.

BMC cancer·2025

Related Experiment Video

Updated: Jul 19, 2026

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
08:07

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma

Published on: April 12, 2019

Synchronous multifocal osteosarcoma: report of one case.

Ming-Horng Tsai1, Chao-Ping Yang, Tang-Her Jaing

  • 1Department of Pediatrics, Chang Gung Children's Hospital, Taoyuan, Taiwan.

Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|November 3, 2006
PubMed
Summary

Synchronous multifocal osteosarcoma (SMOS) is a rare childhood bone cancer with a poor prognosis. This case highlights the aggressive nature of SMOS, even without lung metastasis, leading to rapid disease progression.

More Related Videos

Modeling Osteosarcoma Using Li-Fraumeni Syndrome Patient-derived Induced Pluripotent Stem Cells
08:52

Modeling Osteosarcoma Using Li-Fraumeni Syndrome Patient-derived Induced Pluripotent Stem Cells

Published on: June 13, 2018

Establishment of Cancer Stem Cell Cultures from Human Conventional Osteosarcoma
09:25

Establishment of Cancer Stem Cell Cultures from Human Conventional Osteosarcoma

Published on: October 14, 2016

Related Experiment Videos

Last Updated: Jul 19, 2026

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
08:07

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma

Published on: April 12, 2019

Modeling Osteosarcoma Using Li-Fraumeni Syndrome Patient-derived Induced Pluripotent Stem Cells
08:52

Modeling Osteosarcoma Using Li-Fraumeni Syndrome Patient-derived Induced Pluripotent Stem Cells

Published on: June 13, 2018

Establishment of Cancer Stem Cell Cultures from Human Conventional Osteosarcoma
09:25

Establishment of Cancer Stem Cell Cultures from Human Conventional Osteosarcoma

Published on: October 14, 2016

Area of Science:

  • Oncology
  • Pediatric Oncology
  • Skeletal Biology

Background:

  • Synchronous multifocal osteosarcoma (SMOS) is a rare variant of osteosarcoma characterized by multiple bone lesions at initial presentation.
  • SMOS typically affects children and adolescents and is often associated with a dismal prognosis, even without pulmonary metastasis.
  • The origin of SMOS, whether multicentric or metastatic, remains a subject of debate.

Observation:

  • A case of SMOS in a 10-year-old girl is presented.
  • The primary tumor was a sclerotic lesion in the right distal femur.
  • The patient presented without pulmonary metastasis.

Findings:

  • Despite aggressive multimodal treatment including chemotherapy and limb salvage surgery, the patient experienced rapid disease progression.
  • The progression involved multiple axial skeletal sites and symmetrical long bone lesions.
  • Death occurred within one year of diagnosis, with no evidence of pulmonary metastasis prior to death.

Implications:

  • This case underscores the aggressive behavior and poor prognosis associated with SMOS, even in the absence of pulmonary metastases.
  • It highlights the challenges in managing SMOS and the need for further research into its pathogenesis and optimal treatment strategies.
  • Understanding the behavior of SMOS is crucial for improving outcomes in pediatric bone cancer patients.