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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.
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Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
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Regulation of Expression at Multiple Steps01:23

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The gene expression in cells is regulated at different stages: (i) transcription, (ii) RNA processing, (iii) RNA localization, and (iv) translation. Transcriptional regulation is mediated by regulatory proteins such as transcription factors, activators, or repressors—these control gene expression by initiating or inhibiting the transcription of genes. Once a precursor or pre-mRNA is produced, it undergoes post-transcriptional modification, including 5' capping, splicing, and the...
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The Ras Gene02:38

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The Ras-gene-encoded proteins are regulators of signaling pathways controlling cell proliferation, differentiation, or cell survival. The Ras-gene family in humans constitutes three primary members—the HRas, NRas, and KRas. These genes code for four functionally distinct yet closely related proteins—the HRas, NRas, KRas4A, and KRas4B. The involvement of mutant Ras genes in human cancer was first discovered in 1982 and is among the most common causes of human tumorigenesis.
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Cell Specific Gene Expression01:58

Cell Specific Gene Expression

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Multicellular organisms contain a variety of structurally and functionally distinct cell types, but the DNA in all the cells originated from the same parent cells. The differences in the cells can be attributed to the differential gene expression. Liver cells, whose functions include detoxification of blood, production of bile to metabolize fats, and synthesis of proteins essential for metabolism, must express a specific set of genes to perform their functions. Gene expression also varies with...
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MicroRNAs01:22

MicroRNAs

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MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
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Related Experiment Video

Updated: Jan 7, 2026

An Enrichment Method for Small Extracellular Vesicles Derived from Liver Cancer Tissue
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An Enrichment Method for Small Extracellular Vesicles Derived from Liver Cancer Tissue

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Ribosomal Protein RPL29 Promotes Hepatocellular Carcinoma Progression Through Regulation the Expression of Exosome

Xiaoxue Wang1, Zexin Zhu2

  • 1Department of Dermatology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

Biological Procedures Online
|January 4, 2026
PubMed
Summary
This summary is machine-generated.

Ribosomal protein RPL29 promotes hepatocellular carcinoma (HCC) progression and metastasis by upregulating EXOSC4. Targeting RPL29 or EXOSC4 offers a new therapeutic strategy for primary liver cancer (PLC).

Keywords:
EXOSC4Hepatocellular carcinomaProgressionRPL29

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Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • Primary liver cancer (PLC) presents significant therapeutic challenges.
  • The role and mechanisms of ribosomal protein (RP) RPL29 in hepatocellular carcinoma (HCC) progression are largely unknown.

Purpose of the Study:

  • To investigate the expression, prognostic value, and functional role of RPL29 in HCC.
  • To elucidate the underlying molecular mechanisms of RPL29 in HCC progression and metastasis.

Main Methods:

  • Bioinformatics and immunohistochemistry to assess RPL29 expression and prognostic value in HCC.
  • Gene manipulation (siRNA, cDNA) to study RPL29's effect on HCC cell viability and invasion.
  • Western blot and xenograft models to explore RPL29's function in regulating HCC malignancy.
  • Screening of small molecule drugs targeting EXOSC4.

Main Results:

  • RPL29 expression is significantly elevated in HCC tissues and correlates with poorer patient survival.
  • RPL29 promotes HCC cell proliferation and metastasis, partly by enhancing Exosome Component 4 (EXOSC4) expression.
  • Both RPL29 and EXOSC4 are overexpressed in HCC and associated with adverse outcomes.
  • RPL29 overexpression can rescue proliferation and invasion in EXOSC4-silenced HCC cells.

Conclusions:

  • RPL29 facilitates HCC progression and metastasis by regulating EXOSC4 expression.
  • RPL29 and EXOSC4 represent potential therapeutic targets for HCC treatment.