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"Yang, Zhen"
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PIWIL1 promotes gastric cancer via a piRNA-independent mechanism
Targeted cancer therapy aims to achieve specific elimination of cancerous but not normal cells. Recently, PIWI proteins, a subfamily of the PAZ-PIWI domain (PPD) protein family, have emerged as promising candidates for targeted cancer therapy. PPD proteins are essential for small noncoding RNA pathways. The Argonaute subfamily partners with microRNA and small interfering RNA, whereas the PIWI subfamily partners with PIWI-interacting RNA (piRNA). Both PIWI proteins and piRNA are mostly expressed in the germline and best known for their function in transposon silencing, with no detectable function in mammalian somatic tissues. However, PIWI proteins become aberrantly expressed in multiple types of somatic cancers, thus gaining interest in targeted therapy. Despite this, little is known about the regulatory mechanism of PIWI proteins in cancer. Here we report that one of the four PIWI proteins in humans, PIWIL1, is highly expressed in gastric cancer tissues and cell lines. Knocking out the PIWIL1 gene (PIWIL1-KO) drastically reduces gastric cancer cell proliferation, migration, metastasis, and tumorigenesis. RNA deep sequencing of gastric cancer cell line SNU-1 reveals that KO significantly changes the transcriptome, causing the up-regulation ofmost of its associated transcripts. Surprisingly, few bona fide piRNAs exist in gastric cancer cells. Furthermore, abolishing the piRNA-binding activity of PIWIL1 does not affect its oncogenic function. Thus, PIWIL1 function in gastric cancer cells is independent of piRNA. This piRNA-independent regulation involves interaction with the UPF1-mediated nonsense-mediated mRNA decay (NMD) mechanism. Altogether, our findings reveal a piRNA-independent function of PIWIL1 in promoting gastric cancer.
Journal Article
A high-performance topological bulk laser based on band-inversion-induced reflection
Topological insulators are materials that behave as insulators in the bulk and as conductors at the edge or surface due to the particular configuration of their bulk band dispersion. However, up to date possible practical applications of this band topology on materials’ bulk properties have remained abstract. Here, we propose and experimentally demonstrate a topological bulk laser. We pattern semiconductor nanodisk arrays to form a photonic crystal cavity showing topological band inversion between its interior and cladding area. In-plane light waves are reflected at topological edges forming an effective cavity feedback for lasing. This band-inversion-induced reflection mechanism induces single-mode lasing with directional vertical emission. Our topological bulk laser works at room temperature and reaches the practical requirements in terms of cavity size, threshold, linewidth, side-mode suppression ratio and directionality for most practical applications according to Institute of Electrical and Electronics Engineers and other industry standards. We believe this bulk topological effect will have applications in near-field spectroscopy, solid-state lighting, free-space optical sensing and communication.The interface between photonic crystals with distinct in-band topologies confines electromagnetic modes and gives rise to lasing emission in the bulk.
Journal Article
Eight outcasts : social and political marginalization in China under Mao
\"The 1949 Communist Revolution marked a period of earthshaking change in China. Political, economic, ideological, and cultural movements set into motion came to galvanize the country, culminating in dramatic social transformations at all levels but also in the persecution of hundreds of thousands of the country's citizens. Based on normally inaccessible records of confessions, interrogations, trial transcripts, and depositions, Eight Outcasts tells the stories of eight victims of the Maoist dictatorship. It introduces readers to individuals accused of infractions such as corruption, political wrong thoughts, homosexuality, illicit sexual activity, foreign ties, or \"historical problems\" (connections to the former Kuomintang regime) in the period between the revolution and Mao's death in 1976. Each chapter brings stories of China's voiceless citizens to light, broadening our knowledge of this important transitional period\"--Provided by publisher.
Book
The Circular RNA Interacts with STAT3, Increasing Its Nuclear Translocation and Wound Repair by Modulating Dnmt3a and miR-17 Function
Delayed or impaired wound healing is a major health issue worldwide, especially in patients with diabetes and atherosclerosis. Here we show that expression of the circular RNA circ-Amotl1 accelerated healing process in a mouse excisional wound model. Further studies showed that ectopic circ-Amotl1 increased protein levels of Stat3 and Dnmt3a. The increased Dnmt3a then methylated the promoter of microRNA miR-17, decreasing miR-17-5p levels but increasing fibronectin expression. We found that Stat3, similar to Dnmt3a and fibronectin, was a target of miR-17-5p. Decreased miR-17-5p levels would increase expression of fibronectin, Dnmt3a, and Stat3. All of these led to increased cell adhesion, migration, proliferation, survival, and wound repair. Furthermore, we found that circ-Amotl1 not only increased Stat3 expression but also facilitated Stat3 nuclear translocation. Thus, the ectopic expressed circ-Amotl1 and Stat3 were mainly translocated to nucleus. In the presence of circ-Amotl1, Stat3 interacted with Dnmt3a promoter with increased affinity, facilitating Dnmt3a transcription. Ectopic application of circ-Amotl1 accelerating wound repair may shed light on skin wound healing clinically.
Yang et al. show that expression of the circular RNA circ-Amotl1 accelerated wound healing and increased levels of Stat3 and Dnmt3a. The increased Dnmt3a methylated miR-17 promoter, decreasing miR-17-5p levels but increasing fibronectin expression. Furthermore, circ-Amotl1 facilitated Stat3 nuclear translocation to promote cell activities and wound repair.
Journal Article
Subepicardial endothelial cells invade the embryonic ventricle wall to form coronary arteries
Coronary arteries bring blood flow to the heart muscle. Understanding the developmental program of the coronary arteries provides insights into the treatment of coronary artery diseases. Multiple sources have been described as contributing to coronary arteries including the proepicardium, sinus venosus （SV）, and endocardium. However, the developmental origins of coronary vessels are still under intense study. We have produced a new genetic tool for studying coronary development, an AplnCreER mouse line, which expresses an inducible Cre recombinase specifically in developing coronary vessels. Quantitative analysis of coronary development and timed induction of AplnCreER fate tracing showed that the progenies of subepicardial endothelial cells （ECs） both invade the compact myocardium to form coronary arteries and remain on the surface to produce veins. We found that these subepicardial ECs are the major sources of intramyocardial coronary vessels in the developing heart. In vitro explant assays indicate that the majority of these subepicardial ECs arise from endocardium of the SV and atrium, but not from ventricular endocardium. Clonal analysis of Apln-positive cells indicates that a single subepicardial EC contributes equally to both coronary arteries and veins. Collectively, these data suggested that subepieardial ECs are the major source of intramyocardial coronary arteries in the ventricle wall, and that coronary arteries and veins have a common origin in the developing heart.
Journal Article
A phosphatidic acid-binding lncRNA SNHG9 facilitates LATS1 liquid–liquid phase separation to promote oncogenic YAP signaling
Long noncoding RNAs (lncRNAs) are emerging as a new class of important regulators of signal transduction in tissue homeostasis and cancer development. Liquid–liquid phase separation (LLPS) occurs in a wide range of biological processes, while its role in signal transduction remains largely undeciphered. In this study, we uncovered a lipid-associated lncRNA, small nucleolar RNA host gene 9 (
SNHG9
) as a tumor-promoting lncRNA driving liquid droplet formation of Large Tumor Suppressor Kinase 1 (LATS1) and inhibiting the Hippo pathway. Mechanistically,
SNHG9
and its associated phosphatidic acids (PA) interact with the C-terminal domain of LATS1, promoting LATS1 phase separation and inhibiting LATS1-mediated YAP phosphorylation. Loss of
SNHG9
suppresses xenograft breast tumor growth. Clinically, expression of
SNHG9
positively correlates with YAP activity and breast cancer progression. Taken together, our results uncover a novel regulatory role of a tumor-promoting lncRNA (i.e.,
SNHG9
) in signal transduction and cancer development by facilitating the LLPS of a signaling kinase (i.e., LATS1).
Journal Article
A review of performance improvement strategies for graphene oxide-based and graphene-based membranes in water treatment
In the past few decades, due to the rapid development of industry and the rapid growth of population, emissions of pollutants to the environment have increased dramatically, and the demand for drinking water is also increasing. Water treatment is a matter of concern because it is directly related to the health of humans and wildlife. Graphene and its derivatives have potential applications in seawater desalination and wastewater treatment due to their unique pore structure and ionic molecular sieving separation capabilities. Graphene, graphene oxide (GO), and reduced graphene oxide (rGO) can be formulated into nanoporous materials and composites with tunable properties that can be optimized for water filtration. Methods for perforating graphene include ion etching/ion bombardment and electron beam nanometer engraving, which are briefly introduced in this paper. Graphene-based composites further expand the capabilities of graphene in seawater desalination and wastewater treatment, by introducing new features and properties. In this review, the performance improvement of graphene-based separation membranes in decontamination and desalination in recent years is reviewed in detail. This review focuses on improving the performance of graphene-based membranes for separation, decontamination, and seawater desalination applications, by discussing how various modifications and preparation methods impact important performance properties, including water permeance, selectivity, rejection of solutes, membrane mechanical strength, and antifouling characteristics. We also discuss the outlook for future development of graphene-based membranes.
Journal Article