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Related Concept Videos

Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
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...
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...
Induced Pluripotent Stem Cells01:06

Induced Pluripotent Stem Cells

Stem cells are undifferentiated cells that divide and produce different cell types. Ordinarily, cells that have differentiated into a specific cell type are terminally differentiated; however, scientists have found a way to reprogram these mature cells so that they dedifferentiate and return to an unspecialized, proliferative state. These cells are pluripotent like embryonic stem cells—able to produce all cell types—and are called induced pluripotent stem cells (iPSCs).
Somatic cells are...
Cancer-Critical Genes I: Proto-oncogenes01:33

Cancer-Critical Genes I: Proto-oncogenes

Genes usually encode proteins necessary for the proper functioning of a healthy cell. Mutations can often cause changes to the gene expression pattern, thereby altering the phenotype.
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...

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Tracking Tumor Cell Dissemination from Lung Metastases Using Photoconversion
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Published on: July 7, 2023

Mapping cancer origins.

Richard J Gilbertson1

  • 1Department of Developmental Neurobiology and Oncology, St Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105, USA. richard.gilbertson@stjude.org

Cell
|April 5, 2011
PubMed
Summary
This summary is machine-generated.

Cancer is a diverse disease killing millions annually. Integrating genomic and stem cell technologies offers a promising new approach to developing cures for all cancer patients.

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Area of Science:

  • Oncology
  • Genomics
  • Stem Cell Biology

Background:

  • Cancer represents a complex group of over 200 diseases with significant global mortality.
  • Current therapeutic strategies are hindered by a lack of comprehensive understanding of cancer's heterogeneity.

Purpose of the Study:

  • To explore the potential of integrating genomic and stem cell technologies to overcome challenges in cancer research.
  • To identify novel therapeutic avenues for diverse cancer types.

Main Methods:

  • Review and synthesis of recent advancements in cancer genomics.
  • Analysis of stem cell-based therapeutic approaches in preclinical and clinical settings.
  • Integration of multi-omics data with stem cell biology principles.

Main Results:

  • Genomic profiling reveals critical insights into cancer driver mutations and pathways.
  • Stem cell technologies offer potential for targeted drug delivery and regenerative medicine in cancer.
  • Combined genomic and stem cell approaches show promise in modeling and treating complex cancers.

Conclusions:

  • The convergence of genomics and stem cell technologies presents a powerful strategy to address cancer's diversity.
  • This integrated approach is crucial for advancing precision medicine and achieving a cure for every patient.
  • Further research is warranted to fully translate these integrated technologies into clinical practice.