Related Experiment Video
Updated: May 3, 2026

12:21
MicroRNA In situ Hybridization for Formalin Fixed Kidney Tissues
Published on: November 30, 2013
14.2K
Regulatory feedback loop between T3 and microRNAs in renal cancer
J Boguslawska1, A Piekielko-Witkowska1, A Wojcicka1
1Department of Biochemistry and Molecular Biology, The Centre of Postgraduate Medical Education, Warsaw, Poland.
Molecular and Cellular Endocrinology
|January 21, 2014
Summary
Thyroid hormone signaling influences microRNA expression in renal cancer. This study reveals a feedback loop where microRNAs regulate thyroid hormone pathway genes, and thyroid hormone, in turn, controls microRNA levels.
Area of Science:
- Molecular Biology
- Endocrinology
- Cancer Research
Background:
- MicroRNAs (miRNAs) are short, non-coding RNAs regulating gene expression and impacting physiological processes like hormonal regulation.
- Thyroid hormone signaling plays a crucial role in various bodily functions, and its dysregulation is implicated in diseases like cancer.
Purpose of the Study:
- To investigate the hypothesis that microRNAs targeting thyroid hormone pathway genes are regulated by thyroid hormone signaling.
- To elucidate the mutual regulatory relationship between the triiodothyronine (T3) pathway and the miR-224/miR-452/GABRE cluster in renal cancer.
Main Methods:
- Analysis of the direct regulation of thyroid hormone receptor TRβ1 by miR-452 in renal cancer cells.
- Assessment of the influence of T3 treatment and TR silencing on the expression of the miR-224/452/GABRE cluster and other TRβ1-targeting miRNAs.
- Correlation analysis of miR-452 expression with intracellular T3 concentrations in renal tumors.
Main Results:
- MiR-452 was identified as a direct regulator of thyroid hormone receptor TRβ1 expression in renal cancer cells.
- The expression of the miR-224/452/GABRE cluster and other TRβ1-targeting miRNAs was modulated by T3 treatment and/or TR silencing.
- A positive correlation was observed between miR-452 expression levels and intracellular T3 concentrations within renal tumors.
Conclusions:
- A novel feedback mechanism involving microRNAs and thyroid hormone signaling in renal cancer is proposed.
- MicroRNAs regulate the expression of T3 pathway genes, and conversely, T3 signaling influences microRNA expression, creating a regulatory loop.
Related Concept Videos
mTOR Signaling and Cancer Progression
3.6K
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...
The mTOR pathway or the...
3.6K
mTOR Signaling and Cancer Progression
1.5K
1.5K
MicroRNAs
21.1K
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...
21.1K
MicroRNAs
3.0K
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...
3.0K
PI3K/mTOR/AKT Signaling Pathway
5.1K
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...
5.1K
Master Transcription Regulators
6.1K
Master transcription regulators are regulatory proteins that are predominantly responsible for regulating the expression of multiple genes. Often these genes work in concert to drive a complex process. Activation of a master transcription regulator can lead to a cascade of transcriptional activation necessary for that outcome. These regulators can directly bind to the regulatory sequences of the various genes involved, or they can indirectly regulate transcription by binding to regulatory...
6.1K

