Oncogene-triggered suppression of DNA repair leads to DNA instability in cancer

DNA instability is an important contributor to cancer development. Previously, defects in the chromosome segregation and excessive DNA double strand breaks due to the replication or oxidative stresses were implicated in DNA instability in cancer. Here, we demonstrate that DNA instability can directly result from the oncogene-induced senescence signaling. Expression of the activated form of Her2 oncogene, NeuT, in immortalized breast epithelial cells led to downregulation of the major DNA repair factor histone H2AX and a number of other components of the HR and NHEJ double strand DNA breaks repair pathways. H2AX expression was regulated at the transcriptional level via a senescence pathway involving p21-mediated regulation of CDK and Rb1. The p21-dependent downregulation of H2AX was seen both in cell culture and the MMTV-neu mouse model of Her2-positive breast cancer. Importantly, downregulation of H2AX upon Her2/NeuT expression impaired repair of double strand DNA breaks. This impairment resulted in both increased DNA instability in the form of somatic copy number alterations, and in increased sensitivity to the chemotherapeutic drug doxorubicin. Overall, these findings indicate that the Her2/NeuT oncogene signaling directly potentiates DNA instability and increases sensitivity to DNA damaging treatments

Hormander class of pseudo-differential operators on compact Lie groups and global hypoellipticity

In this paper we give several global characterisations of the Hormander class of pseudo-differential operators on compact Lie groups. The result is applied to give criteria for the ellipticity and the global hypoellipticity of pseudo-differential operators in terms of their matrix-valued full symbols. Several examples of the first and second order globally hypoelliptic differential operators are given. Where the global hypoelliptiticy fails, one can construct explicit examples based on the analysis of the global symbols.Comment: 20 page

HIV-1 Vpr Enhances Viral Burden by Facilitating Infection of Tissue Macrophages but Not Nondividing CD4+ T Cells

Prior experiments in explants of human lymphoid tissue have demonstrated that human immunodeficiency virus type 1 (HIV-1) productively infects diverse cellular targets including T cells and tissue macrophages. We sought to determine the specific contribution of macrophages and T cells to the overall viral burden within lymphoid tissue. To block infection of macrophages selectively while preserving infection of T cells, we used viruses deficient for viral protein R (Vpr) that exhibit profound replication defects in nondividing cells in vitro. We inoculated tonsil histocultures with matched pairs of congenic viruses that differed only by the presence of a wild-type or truncated vpr gene. Although these viruses exhibited no reduction in the infection or depletion of T cells, the ability of the Vpr-deficient R5 virus to infect tissue macrophages was severely impaired compared with matched wild-type R5 virus. Interestingly, the Vpr-deficient R5 virus also exhibited a 50% reduction in overall virus replication compared with its wild-type counterpart despite the fact that macrophages represent a small fraction of the potential targets of HIV-1 infection in these tissues. Collectively, these data highlight the importance of tissue macrophages in local viral burden and further implicate roles for CC chemokine receptor 5, macrophages, and Vpr in the life cycle and pathogenesis of HIV-1

Fluctuating charge density waves in the Hubbard model

The charge susceptibility of the two-dimensional repulsive Hubbard model is investigated using the diagram technique developed for the case of strong correlations. In this technique, a power series in the hopping constant is used. It is shown that once the Fermi level crosses one of the Hubbard subbands a sharp peak appears in the momentum dependence of the static susceptibility. With further departure from half-filling the peak transforms to a ridge around the $\Gamma$ point. In the considered range 0\leq|1-\bar{n}|\alt 0.2 of the electron filling $\bar{n}$ the static susceptibility is finite which points to the absence of the long-range charge ordering. However, for $|1-\bar{n}|\approx 0.12$ the susceptibility maxima are located halfway between the center and the boundaries of the Brillouin zone. In this case an interaction of carriers with tetragonal distortions can stabilize the charge density wave with the wavelength of four lattice spacings, as observed experimentally in the low-temperature tetragonal phase of lanthanum cuprates. In the range of parameters inherent in cuprate perovskites the character of the susceptibility evolution with $\bar{n}$ depends only weakly on the ratio of the nearest-neighbor hopping constant to the Hubbard repulsion and on details of the initial band structure. The location of the susceptibility maxima in the Brillouin zone is mainly determined by the value of $\bar{n}$.Comment: 8 pages, 4 figure