Tomato paste alters NF-κB and cancer-related mRNA expression in prostate cancer cells, xenografts, and xenograft

Marit Kolberg1, Sigrid Pedersen, Nasser E Bastani

  • 1a Department of Nutrition, Institute of Basic Medical Sciences, Faculty of Medicine , University of Oslo , Oslo , Norway.

Nutrition and Cancer
|February 10, 2015
PubMed

Insights

Tomatoes show biological activity against cancer-related inflammation by modulating nuclear factor-kappa B (NF-κB) signaling. This study investigated tomato paste

Area of Science:

  • Oncology
  • Nutritional Science
  • Molecular Biology

Background:

  • Prostate cancer development may be mitigated by tomatoes, potentially via nuclear factor-kappa B (NF-κB) signaling pathways.
  • Understanding the molecular mechanisms of tomato's chemopreventive potential is crucial.

Purpose of the Study:

  • To investigate the effects of tomato paste on NF-κB activity and cancer-related gene expression in prostate cancer cells and xenografts.
  • To determine if dietary tomato paste influences NF-κB signaling and gene expression in vivo.

Main Methods:

  • Human prostate cancer cells (PC3) with an NF-κB-luciferase construct were treated with tomato extracts.
  • Mice bearing PC3 xenografts were fed a Western-like diet with or without 10% tomato paste.
  • NF-κB activity, gene expression, and lycopene accumulation were analyzed.

Main Results:

  • Tomato diet significantly inhibited TNFα-stimulated NF-κB activity in cultured PC3 cells.
  • Dietary tomato paste modulated genes related to inflammation, apoptosis, and cancer progression in xenografts.
  • Lycopene accumulated in tissues and serum of mice on the tomato diet; NF-κB activity showed a trend toward inhibition in xenografts.

Conclusions:

  • Tomatoes possess biological activity relevant to cancer-related inflammation.
  • Tomato consumption may influence key signaling pathways and gene expression in the tumor microenvironment.
  • Further research into tomato-based cancer prevention strategies is warranted.

Related Concept Videos

The Tumor Microenvironment02:17

The Tumor Microenvironment

Every normal cell or tissue is embedded in a complex local environment called stroma, consisting of different cell types, a basal membrane, and blood vessels. As normal cells mutate and develop into cancer cells, their local environment also changes to allow cancer progression. The tumor microenvironment (TME) consists of a complex cellular matrix of stromal cells and the developing tumor. The cross-talk between cancer cells and surrounding stromal cells is critical to disrupt normal tissue...
8.3K
NF-κB-dependent Signaling Pathway02:26

NF-κB-dependent Signaling Pathway

The transcription factor NF-κB was discovered in 1986 in the lab of Nobel laureate Professor David Baltimore, for its interaction with the immunoglobulin light chain enhancer in B-cells. After more than three decades of study, it is now evident that NF-κB regulates the expression of over 100 genes. Most of these genes play an essential role in the innate and adaptive immune responses as well as the inflammatory responses of animals.
NF-κB-dependent Signaling Mechanism
The...
10.9K
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