Berberine (BBR) is a natural alkaloid with significant antitumor activities against many types of cancer cells. This study investigated the molecular mechanisms by which BBR suppresses the growth of HER2-overexpressing breast cancer cells. The results show that BBR induces G1-phase cell cycle arrest by interfering with the expression of cyclins D1 and E and that it induces cellular apoptosis through the induction of a mitochondria/caspase pathway. The data also indicate that BBR inhibits cellular growth and promotes apoptosis by down-regulating the HER2/PI3K/Akt signaling pathway. Furthermore, it is also shown that a combination of taxol and BBR significantly slows the growth rate of HER2-overexpressing breast cancer cells. In conclusion, this study suggests that BBR could be a useful adjuvant therapeutic agent in the treatment of HER2-overexpressing breast cancer.

Berberine (BBR) is a natural alkaloid with significant antitumor activities against many types of cancer cells. In this study, we investigated the molecular mechanisms by which BBR repressed the metastatic potential of breast cancer cells. BBR was found to downregulate the enzymatic activities and expression levels of matrix metalloproteinases 2 and 9 (MMP2 and MMP9, respectively). The BBR-mediated suppression of MMP2 and MMP9 involved the inhibition of the Akt/nuclear factor kappa B (NF-κB) and activator protein-1 (AP-1) signaling pathways. Furthermore, BBR repressed the expression of the Akt protein by modulating the mRNA expression level and protein degradation of Akt. In conclusion, this study suggests that BBR can reduce the metastatic potential of highly metastatic breast cancer cells and may be a useful adjuvant therapeutic agent in the treatment of breast cancer by targeting the Akt pathway.

Interferon-gamma (IFN-gamma) is known to downregulate HER2 oncoprotein (p185(HER2) or briefly p185) in prostate cancer cells. We demonstrate that the IFN-gamma-induced retinoid-inducible gene 1 (RIG1) acts as a transrepressor of p185. Furthermore, we exhibit that RIG1 downregulates the activated (phosphorylated) form of p185 and phosphoinositide-3 kinase (PI3K)/serine/threonine-specific protein kinase (Akt) and the mammalian target of rapamycin (mTOR), downstream substrates of HER2. We also elucidate that heregulin (HRG) specifically restores the activation of p185 and Akt after their activities are reduced by RIG1. Additionally, expression of vascular endothelial growth factor (VEGF) increases through the HER2- and Akt/mTOR-signaling pathways, indicating that VEGF is downregulated by RIG1 within the cell. These findings suggest that RIG1 plays a role in IFN-gamma-mediated therapy by downregulating p185 and its downstream PI3K/Akt/mTOR/VEGF-signaling pathway. These results may provide a new therapeutic mechanism for the clinical use of IFN-gamma and RIG1.

A technique integrating multishot periodically rotated overlapping parallel lines with enhanced reconstruction (PROPELLER) and parallel imaging is presented for diffusion echo-planar imaging (EPI) at high spatial resolution. The method combines the advantages of parallel imaging to achieve accelerated sampling along the phase-encoding direction, and PROPELLER acquisition to further decrease the echo train length (ETL) in EPI. With an eight-element circularly symmetric RF coil, a parallel acceleration factor of 4 was applied such that, when combined with PROPELLER acquisition, a reduction of geometric distortions by a factor substantially greater than 4 was achieved. Because it offers rapid data acquisition and requires only a few RF pulses, single-shot echo-planar imaging (EPI) is generally used as the signal readout for diffusion-weighted MRI (DWI). However, owing to EPI's relatively slow sampling rate along the phase-encoding direction, diffusion images generally exhibit substantial susceptibility-related geometric distortions along the phase-encoding direction, especially around regions that show inhomogeneous magnetic field distributions (1). These distortions can strongly degrade the quality of neurological investigations near the skull base, and may result in a misleading clinical diagnosis (2).Methods to reduce geometric distortion can be divided into at least two different categories. The single-shot approach involves an increase in the bandwidth along the phase-encoding direction (BW PE ) by acquiring sufficient data for image reconstruction with a reduced echo train length (ETL) within one shot. A typical example is parallel imaging employing the use of phased-array RF coils (3,4). In contrast to the single-shot approach, methods in the second category reduce the ETL by splitting the entire data acquisition into multiple shots. In multishot diffusion imaging, the phase difference induced by physiological motion in each shot can lead to severe ghosting artifacts (5), since any motion is transformed into a phase change of the spin isochromats after DW magnetization preparation. Therefore, in multishot DWI, robust correction techniques must accompany the acquisition. One technique that could achieve this aim via inherent navigator correction is the multishot periodically rotated overlapping parallel lines with enhanced reconstruction (PROPELLER) method (6,7).In the present study we integrated the two aforementioned approaches (parallel imaging and PROPELLER acquisition) to obtain multishot high-resolution diffusion images with substantially reduced geometric distortions. We were particularly interested in the PROPELLER imaging method because, as will be shown in a later section, it fills the k-space by using several acquisitions of parallel lines around the center k-space with rotated phase-encoding directions (7). The rotational symmetry of k-space trajectory is especially suitable for parallel imaging acceleration when a circularly symmetric phase array coil is used for signal receiving. In other words,...

Ganoderma, also known as Lingzhi or Reishi, has been used for medicinal purposes in Asian countries for centuries. It is a medicinal fungus with a variety of biological properties including immunomodulatory and antitumor activities. In this study, we investigated the molecular mechanisms by which Ganoderma tsugae (GT), one of the most common species of Ganoderma, inhibits the proliferation of HER2-overexpressing cancer cells. Here, we show that a quality assured extract of GT (GTE) inhibited the growth of HER2-overexpressing cancer cells in vitro and in vivo and enhanced the growth-inhibitory effect of antitumor drugs (e.g., taxol and cisplatin) in these cells. We also demonstrate that GTE induced cell cycle arrest by interfering with the HER2/PI3K/Akt signaling pathway. Furthermore, GTE curtailed the expression of the HER2 protein by modulating the transcriptional activity of the HER2 gene and the stability/degradation of the HER2 protein. In conclusion, this study suggests that GTE may be a useful adjuvant therapeutic agent in the treatment of cancer cells that highly express HER2.