Oncogenic non-coding RNA NEAT1 promotes the prostate cancer cell growth through the SRC3/IGF1R/AKT pathway

Wei Xiong1, Changkun Huang1, Huanghao Deng1

  • 1Department of Urology, The Second Xiangya Hospital, Central South University, Changsha, 410011, China.

Insights

Nuclear Enriched Abundant Transcript 1 (NEAT1) interacts with Steroid Receptor Coactivator 3 (SRC3) to promote prostate cancer growth. This NEAT1/SRC3 interaction upregulates the IGF1R/AKT pathway, driving cancer progression.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Steroid receptor coactivator 3 (SRC3) is an androgen receptor (AR) coactivator implicated in prostate cancer progression.
  • Non-coding RNAs (ncRNAs) are increasingly recognized for their roles in cancer development, but their interaction with AR coactivators remains poorly understood.

Purpose of the Study:

  • To investigate the functional relationship between ncRNA and SRC3 in prostate cancer.
  • To identify specific ncRNAs that interact with SRC3 and elucidate their mechanism of action in prostate cancer cell growth.

Main Methods:

  • Prostate cancer cell lines were used to study the interaction between NEAT1 and SRC3.
  • Western blotting and cell proliferation assays were employed to analyze the effects of NEAT1 on the SRC3/IGF1R/AKT pathway.
  • Expression levels of NEAT1, SRC3, and IGF1R were examined in patient samples.

Main Results:

  • Nuclear Enriched Abundant Transcript 1 (NEAT1) was found to interact with SRC3 in prostate cancer cells.
  • NEAT1 upregulates AKT phosphorylation through the SRC3/IGF1R pathway, thereby promoting prostate cancer cell growth.
  • Elevated expression of NEAT1, SRC3, and IGF1R was observed in prostate cancer patient samples.

Conclusions:

  • NEAT1 is identified as a novel SRC3-binding ncRNA.
  • NEAT1 promotes prostate cancer cell proliferation via the SRC3/IGF1R/AKT signaling pathway.
  • Targeting the NEAT1/SRC3/IGF1R/AKT axis may offer a therapeutic strategy for prostate cancer.

Related Concept Videos

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...
4.9K
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...
5.3K
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...
11.5K
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...
5.7K
The Ras Gene02:38

The Ras Gene

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.
Ras is a...
7.4K
Mitogens and the Cell Cycle02:38

Mitogens and the Cell Cycle

Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
8.2K