Noiseless Linear Amplification and Distillation of Entanglement

The idea of signal amplification is ubiquitous in the control of physical systems, and the ultimate performance limit of amplifiers is set by quantum physics. Increasing the amplitude of an unknown quantum optical field, or more generally any harmonic oscillator state, must introduce noise. This linear amplification noise prevents the perfect copying of the quantum state, enforces quantum limits on communications and metrology, and is the physical mechanism that prevents the increase of entanglement via local operations. It is known that non-deterministic versions of ideal cloning and local entanglement increase (distillation) are allowed, suggesting the possibility of non-deterministic noiseless linear amplification. Here we introduce, and experimentally demonstrate, such a noiseless linear amplifier for continuous-variables states of the optical field, and use it to demonstrate entanglement distillation of field-mode entanglement. This simple but powerful circuit can form the basis of practical devices for enhancing quantum technologies. The idea of noiseless amplification unifies approaches to cloning and distillation, and will find applications in quantum metrology and communications.Comment: Submitted 10 June 200

Dysregulation of MicroRNA-34a Expression in Head and Neck Squamous Cell Carcinoma Promotes Tumor Growth and Tumor Angiogenesis

MicroRNAs (miRs) are small non-coding RNAs that play an important role in cancer development where they can act as oncogenes or as tumor-suppressors. miR-34a is a tumor-suppressor that is frequently downregulated in a number of tumor types. However, little is known about the role of miR-34a in head and neck squamous cell carcinoma (HNSCC).miR-34a expression in tumor samples, HNSCC cell lines and endothelial cells was examined by real time PCR. Lipofectamine-2000 was used to transfect miR-34a in HNSCC cell lines and human endothelial cells. Cell-proliferation, migration and clonogenic survival was examined by MTT, Xcelligence system, scratch assay and colony formation assay. miR-34a effect on tumor growth and tumor angiogenesis was examined by in vivo SCID mouse xenograft model. Our results demonstrate that miR-34a is significantly downregulated in HNSCC tumors and cell lines. Ectopic expression of miR-34a in HNSCC cell lines significantly inhibited tumor cell proliferation, colony formation and migration. miR-34a overexpression also markedly downregulated E2F3 and survivin levels. Rescue experiments using microRNA resistant E2F3 isoforms suggest that miR-34a-mediated inhibition of cell proliferation and colony formation is predominantly mediated by E2F3a isoform. In addition, tumor samples from HNSCC patients showed an inverse relationship between miR-34a and survivin as well as miR-34a and E2F3 levels. Overexpression of E2F3a completely rescued survivin expression in miR-34a expressing cells, thereby suggesting that miR-34a may be regulating survivin expression via E2F3a. Ectopic expression of miR-34a also significantly inhibited tumor growth and tumor angiogenesis in a SCID mouse xenograft model. Interestingly, miR-34a inhibited tumor angiogenesis by blocking VEGF production by tumor cells as well as directly inhibiting endothelial cell functions.Taken together, these findings suggest that dysregulation of miR-34a expression is common in HNSCC and modulation of miR34a activity might represent a novel therapeutic strategy for the treatment of HNSCC

Channel purification via continuous-variable quantum teleportation with Gaussian postselection

We present a protocol based on continuous-variable quantum teleportation and Gaussian postselection that can be used to correct errors introduced by a lossy channel. We first show that the global transformation enacted by the protocol is equivalent to an effective system composed of a noiseless amplification (or attenuation), and an effective quantum channel, which can in theory have no loss and an amount of thermal noise arbitrarily small, hence tending to an identity channel. An application of our protocol is the probabilistic purification of quantum non-Gaussian states using only Gaussian operations

Models of reduced-noise, probabilistic linear amplifiers

We construct an amplifier that interpolates between a nondeterministic, immaculate linear amplifier and a deterministic, ideal linear amplifier and beyond to nonideal linear amplifiers. The construction involves cascading an immaculate linear amplifier that has amplitude gain g1 with a (possibly) nonideal linear amplifier that has gain g2. With respect to normally ordered moments, the device has output noise μ2(G2−1) where G=g1g2 is the overall amplitude gain and μ2 is a noise parameter. When μ2≥1, our devices realize ideal (μ2=1) and nonideal (μ2>1) linear amplifiers. When 0≤μ2<1, these devices work effectively only over a restricted region of phase space and with some subunity success probability p✓. We investigate the performance of our μ2 amplifiers in terms of a gain-corrected probability-fidelity product and the ratio of input to output signal-to-noise ratios corrected for success probability