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Related Concept Videos

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...
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...
Abnormal Proliferation02:23

Abnormal Proliferation

Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter...
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a rapamycin-insensitive companion...
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...

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Related Experiment Video

Updated: May 17, 2026

Assessing Cellular Target Engagement by SHP2 (PTPN11) Phosphatase Inhibitors
08:45

Assessing Cellular Target Engagement by SHP2 (PTPN11) Phosphatase Inhibitors

Published on: July 17, 2020

PNUTS functions as a proto-oncogene by sequestering PTEN.

Sridhar Kavela1, Swapnil R Shinde, Raman Ratheesh

  • 1Laboratory of Cell Death & Cell Survival, Centre for DNA Fingerprinting and Diagnostics (CDFD), Nampally, India.

Cancer Research
|November 3, 2012
PubMed
Summary

Protein phosphatase-1 nuclear targeting subunit PNUTS regulates the tumor suppressor PTEN. PNUTS depletion increases apoptosis and reduces proliferation, suggesting PNUTS is an oncogene in cancer.

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Published on: August 25, 2021

Area of Science:

  • Molecular biology
  • Cancer research
  • Cellular signaling

Background:

  • PTEN is a crucial tumor suppressor gene regulating the PI3K/Akt pathway.
  • PTEN controls cell survival, growth, motility, invasiveness, and angiogenesis.
  • Regulation of PTEN activity in normal and disease states is not fully understood.

Purpose of the Study:

  • To identify novel regulators of PTEN.
  • To investigate the role of PNUTS (PPP1R10) in PTEN regulation.
  • To explore the potential oncogenic role of PNUTS in cancer.

Main Methods:

  • Protein-protein interaction assays to identify PTEN-associated proteins.
  • Immunofluorescence and co-immunoprecipitation to study PTEN-PNUTS interaction.
  • Cellular assays (apoptosis, proliferation) upon PNUTS depletion.
  • Analysis of PNUTS expression in cancer tissues.

Main Results:

  • PNUTS (PPP1R10) was identified as a PTEN-associated protein.
  • PNUTS directly binds to PTEN's C2 domain and sequesters PTEN in the nucleus.
  • Depletion of PNUTS results in PTEN-dependent apoptosis and reduced proliferation.
  • PNUTS expression is elevated in certain cancers compared to normal tissues.

Conclusions:

  • PNUTS is a novel regulator of the tumor suppressor PTEN.
  • PNUTS interaction with PTEN influences PTEN's cellular localization and function.
  • PNUTS acts as a PTEN-dependent oncogene, with elevated expression in cancers.