MiR-345 suppresses proliferation, migration and invasion by targeting Smad1 in human prostate cancer

Qi-guang Chen1, Wei Zhou2, Tao Han3

  • 1Department of Urology, The First Affiliated Hospital of China Medical University, Nanjing Street 155#, Shenyang, 110001, Liaoning, China.

Abstract

Insights

MicroRNA-345 (miR-345) is downregulated in prostate cancer, suppressing tumor growth, migration, and invasion by targeting Smad1. This finding offers new insights into prostate cancer metastasis.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Dysregulated microRNAs (miRNAs) play roles in cancer metastasis, but their specific involvement in prostate cancer remains unclear.
  • This study investigates the expression and function of miR-345 in prostate cancer progression.

Purpose of the Study:

  • To determine the role of miR-345 in prostate cancer proliferation, migration, and invasion.
  • To identify the molecular targets of miR-345 in prostate cancer.

Main Methods:

  • Quantitative real-time PCR to assess miR-345 expression in prostate cancer tissues and cell lines.
  • In vitro assays (proliferation, migration, invasion) to evaluate the functional effects of miR-345.
  • In vivo studies using a nude mice model to assess tumor growth inhibition.
  • Luciferase reporter assays and Western blotting to identify and validate Smad1 as a direct target of miR-345.

Main Results:

  • miR-345 expression was significantly downregulated in prostate cancer tissues and cell lines.
  • Overexpression of miR-345 suppressed prostate cancer cell proliferation, migration, and invasion in vitro.
  • miR-345 inhibited prostate cancer growth in vivo.
  • Smad1 was identified as a direct target of miR-345, and its re-expression rescued the suppressive effects of miR-345 on cell migration and invasion.

Conclusions:

  • miR-345 acts as a tumor suppressor in prostate cancer.
  • The suppressive effects of miR-345 on prostate cancer progression are mediated through the downregulation of Smad1.

Related Concept Videos

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...
5.4K
MicroRNAs01:22

MicroRNAs

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...
4.3K
MicroRNAs01:22

MicroRNAs

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...
24.7K
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...
5.1K
The Retinoblastoma Gene01:20

The Retinoblastoma Gene

Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.9K