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Updated: Feb 17, 2026

Sequencing Small Non-coding RNA from Formalin-fixed Tissues and Serum-derived Exosomes from Castration-resistant Prostate Cancer Patients
Published on: November 19, 2019
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.
Abstract:
Steroid receptor co-activator3 (SRC3) has been known to severe as an androgen receptor (AR) coactivator and is involved in the prostate cancer progression. Non-coding RNA (ncRNA) plays an important role in the cancer progression. However, the mechanism underlying the relationship between ncRNA and AR coactivators is still unclear. Here, we found a ncRNA, Nuclear Enriched Abundant Transcript 1 (NEAT1), was able to interact with SRC3 in the prostate cancer cell lines. NEAT1 can upregulate the AKT phosphorylation via a SRC3/IGF1R pathway. In function, NEAT1 promoted the prostate cancer cell growth through IGF1R/AKT signaling pathway. The NEAT1, SRC3, and IGF1R were highly expressed in the patients' samples of prostate cancer. Therefore, we found a novel SRC3 binding ncRNA that can promote the prostate cancer cell growth through SRC3/IGF1R/AKT pathway.
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.
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