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Targeted Cancer Therapies02:57

Targeted Cancer Therapies

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The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
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Cancer Stem Cells and Tumor Maintenance02:40

Cancer Stem Cells and Tumor Maintenance

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Early diagnosis and treatment can often cure cancer. However, even with treatment, residual cells called cancer stem cells (CSC) might remain, often causing tumor recurrence. These cancer stem cells possess the potential for self-renewal and multi-lineage differentiation and are often responsible for the therapeutic resistance displayed in most cancers.
Cancer stem cells are thought to originate from tissue-specific normal stem cells or progenitor cells. The normal stem cells usually reside in...
5.8K
Combination Therapies and Personalized Medicine02:50

Combination Therapies and Personalized Medicine

5.8K
Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
5.8K
Electron Transport Chain: Complex I and II01:46

Electron Transport Chain: Complex I and II

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The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
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Drugs that Stabilize Microtubules01:15

Drugs that Stabilize Microtubules

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Microtubules are dynamic structures that undergo cycles of catastrophe and rescue. The microtubules play a central role in cell division by forming the spindle apparatus for segregating the chromosomes. This makes them ideal targets for regulating dividing cells in tumors and malignant cancer cells. Microtubule stabilizing drugs help stabilize the microtubule formation and promote its polymerization. Paclitaxel was the first microtubule stabilizing agent used as anticancer drug in chemotherapy...
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Treatment Resistant Cancers02:56

Treatment Resistant Cancers

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Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
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  2. 小分子でがん幹細胞を選択的に根絶するために,臓器膜のk+/h+輸送を媒介する
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  2. 小分子でがん幹細胞を選択的に根絶するために,臓器膜のk+/h+輸送を媒介する

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Harnessing the DNA Dye-triggered Side Population Phenotype to Detect and Purify Cancer Stem Cells from Biological Samples
09:57

Harnessing the DNA Dye-triggered Side Population Phenotype to Detect and Purify Cancer Stem Cells from Biological Samples

Published on: May 10, 2017

7.9K

小分子でがん幹細胞を選択的に根絶するために,臓器膜のK+/H+輸送を媒介する

Fang-Fang Shen1, Sheng-Yao Dai1, Nai-Kei Wong1,2

  • 1Morningside Laboratory for Chemical Biology, Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, China.

Journal of the American Chemical Society
|May 23, 2020

PubMed で要約を見る

まとめ
この要約は機械生成です。

研究者らは,がん細胞を 選択的に標的とする新種の合成カリウム (K+) トランスポーターを開発しました. このトランスポーターはミトコンドリアとリソソームのイオンホメオスタシスを破壊し,がん幹細胞の根絶と腫瘍形成の減少につながります.

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Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics
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Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics

Published on: May 14, 2016

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Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples
07:03

Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples

Published on: October 2, 2020

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関連する実験動画

Harnessing the DNA Dye-triggered Side Population Phenotype to Detect and Purify Cancer Stem Cells from Biological Samples
09:57

Harnessing the DNA Dye-triggered Side Population Phenotype to Detect and Purify Cancer Stem Cells from Biological Samples

Published on: May 10, 2017

7.9K
Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics
06:00

Through the Looking Glass: Time-lapse Microscopy and Longitudinal Tracking of Single Cells to Study Anti-cancer Therapeutics

Published on: May 14, 2016

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Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples
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Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples

Published on: October 2, 2020

4.9K

科学分野:

  • 生物化学
  • 細胞生物学
  • 腫瘍学

背景:

  • 細胞のイオンホメオスタシスを破壊することは,がん治療の治療戦略です.
  • これまでの合成イオントランスポーターは 選択性が欠けていて 健康な細胞と癌細胞に 毒性をもたらしました

研究 の 目的:

  • がん治療のための選択的な合成カリウム (K+) トランスポーターを開発する.
  • 選択性イオン輸送のメカニズムと癌幹細胞 (CSC) に与える影響を調査する.

主な方法:

  • サイト選択的なK+/H+輸送のための内生的なpHグラディエントと膜ポテンシャルを利用した.
  • 生きている細胞のミトコンドリアとリソソーム膜を標的とする.
  • 化学療法に抵抗する卵巣がん幹細胞 (CSC) とマウスの腫瘍形成における評価された細胞毒性.

主要な成果:

  • 合成K + トランスポーターは,ミトコンドリアとリソソーム膜にサイト選択的なK + / H + トランスポートを示した.
  • 誘発されたミトコンドリアとリソソムの損傷により,化学療法に耐性のある卵巣がん幹細胞 (CSCs) に対する細胞毒性が最大47倍に増加します.
  • CSCのオートファギーの抑制とアポトーシスの誘発
  • CSCの根絶は,体内で腫瘍の形成を鈍化させた.

結論:

  • 開発された合成K+トランスポーターは,細胞イオングラデーションを利用して,がん細胞を標的とする選択的なアプローチを提供します.
  • この戦略は,がんやその他のイオンチャネル機能障害を含む疾患の治療のための次世代の合成カチオントランスポーターの開発の可能性を示しています.