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The Tumor Microenvironment02:17

The Tumor Microenvironment

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Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
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Animal Mitochondrial Genetics02:59

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Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
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Export of Mitochondrial and Chloroplast Genes02:19

Export of Mitochondrial and Chloroplast Genes

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A eukaryotic cell can have up to three different types of genetic systems: nuclear, mitochondrial, and chloroplast. During evolution, organelles have exported many genes to the nucleus; this transfer is still ongoing in some plant species. Approximately 18% of the Arabidopsis thaliana nuclear genome is thought to be derived from the chloroplast’s cyanobacterial ancestor, and around 75% of the yeast genome derived from the mitochondria’s bacterial ancestor. This export has occurred...
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Comparing Mitochondrial, Chloroplast, and Prokaryotic Genomes02:16

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The present-day mitochondrial and chloroplast genomes have retained some of the characteristics of their ancestral prokaryotes and also have acquired new attributes during their evolution within eukaryotic cells. Like prokaryotic genomes, mitochondrial and chloroplast genomes neither bind with histone-like proteins nor show complex packaging into chromosome-like structures, as observed in eukaryotes. Unlike mitotic cell divisions observed in eukaryotic cells, mitochondria and chloroplasts...
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The Inner Mitochondrial Membrane01:28

The Inner Mitochondrial Membrane

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The inner mitochondrial membrane is the primary site of ATP synthesis. The inner membrane domain that forms a smooth layer adjacent to the outer membrane is called the inner boundary membrane. This domain contains membrane transporters that drive metabolites in and out of the mitochondria.  In contrast, the inner membrane network that invaginates into the matrix space is called the cristae membrane. This domain accounts for principle mitochondrial function as it accommodates the protein...
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Mitochondrial Membranes01:45

Mitochondrial Membranes

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A single mitochondrion is a bean-shaped organelle enclosed by a double-membrane system. The outer membrane of mitochondria is smooth and contains many porins - the integral membrane transporters. Porins enable free diffusion of ions and small uncharged molecules through the outer mitochondrial membrane but limit the transport of molecules larger than 5000 Daltons. Further, the outer mitochondrial membrane forms a unique structure called membrane contact sites with other subcellular organelles,...
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Related Experiment Video

Updated: Feb 14, 2026

Enrichment and Characterization of the Tumor Immune and Non-immune Microenvironments in Established Subcutaneous Murine Tumors
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Enrichment and Characterization of the Tumor Immune and Non-immune Microenvironments in Established Subcutaneous Murine Tumors

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Mitochondrial Transfer in the Tumor Microenvironment.

Ryo Omae1,2, Takamasa Ishino1, Yosuke Togashi1,3,4

  • 1Department of Tumor Microenvironment, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.

Cancer Science
|February 13, 2026
PubMed
Summary
This summary is machine-generated.

Mitochondria transfer between cells, impacting cancer progression and immune response. Targeting this process offers potential new cancer therapies.

Keywords:
antitumor immunitycell‐to‐cell interactionmitochondriamitochondrial transfertumor microenvironment

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Area of Science:

  • Cell Biology
  • Cancer Research
  • Immunology

Background:

  • Mitochondria are crucial organelles involved in energy production, metabolism, apoptosis, and inflammation.
  • Mitochondrial transfer between cells is a newly recognized phenomenon with significant implications in the tumor microenvironment.
  • Existing research highlights the functional relevance of mitochondrial transfer in cancer development and progression.

Purpose of the Study:

  • To explore the mechanisms and functional significance of mitochondrial transfer in the context of cancer.
  • To investigate the role of mitochondrial transfer in tumor cell adaptation and therapeutic resistance.
  • To examine the impact of mitochondrial transfer on antitumor immunity within the tumor microenvironment.

Main Methods:

  • Review of recent studies on mitochondrial transfer mechanisms, including tunneling nanotubes and extracellular vesicles.
  • Analysis of regulatory factors such as Miro1/2, connexin 43, ICAM-1, VCAM-1, and reactive oxygen species.
  • Examination of evidence regarding mitochondrial transfer's influence on tumor cell metabolism, therapeutic evasion, and T cell function.

Main Results:

  • Mitochondrial transfer can occur via tunneling nanotubes and extracellular vesicles, regulated by specific molecular pathways.
  • Tumor cells may acquire mitochondria from surrounding cells to adapt to metabolic stress and resist therapies.
  • Transfer of mitochondria from tumor cells to T cells can suppress antitumor immune responses.

Conclusions:

  • Mitochondrial transfer is a key process in the tumor microenvironment, influencing both tumor progression and immune evasion.
  • Targeting mitochondrial transfer presents a promising novel therapeutic strategy for improving cancer treatment outcomes.
  • Further research is needed to develop safe and specific in vivo methods for manipulating mitochondrial transfer.