Amplifying colorectal cancer progression: impact of a PDIA4/SP1 positive feedback loop by circPDIA4 sponging miR-9-5p

Objective:Colorectal cancer(CRC)is a prevalent malignant tumor with a high fatality rate.CircPDIA4 has been shown to have a vital role in cancer development by acting as a facilitator.Nevertheless,the impact of the circPDIA4/miR-9-5p/SP1 axis on development of CRC has not been studied.Methods:Western blot,immunohistochemistry,and reverse transcription-quantitative polymerase chain reaction assays were used to analyze gene expression.The CCK-8 assay was used to assess cell growth.The Transwell assay was used to detect invasion and migration of cells.The luciferase reporter and RNA immunoprecipitation tests were used to determine if miR-9-5p and circPDIA4(or SP1)bind to one another.An in vivo assay was used to measure tumor growth.Results:It was shown that circPDIA4 expression was greater in CRC cell lines and tissues than healthy cell lines and tissues.CircPDIA4 knockdown prevented the invasion,migration,and proliferation of cells in CRC.Additionally,the combination of circPDIA4 and miR-9-5p was confirmed,as well as miR-9-5p binding to SP1.Rescue experiments also showed that the circPDIA4/miR-9-5p/SP1 axis accelerated the development of CRC.In addition,SP1 combined with the promoter region of circPDIA4 and induced circPDIA4 transcription.CircPDIA4 was shown to facilitate tumor growth in an in vivo assay.Conclusions:The circPDIA4/miR-9-5p/SP1 feedback loop was shown to aggravate CRC progression.This finding suggests that the ceRNA axis may be a promising biomarker for CRC patient treatment.

Chromosome-level genome assembly of the dotted gizzard shad(Konosirus punctatus) provides insights into its adaptive evolution

Konosirus punctatus is an economically important marine fishery resource and is widely distributed from the Indian to Pacific oceans.It is a good non-model species for genetic studies on salinity and temperature adaptation.However,a high-quality reference genome has not yet been reported.

Characterization and ultraviolet-visible shielding property of samarium-cerium compounds containing Sm_(2)O_(2)S prepared by co-precipitation method

Since ultraviolet(UV)light,as well as blue light,which is part of visible light,is harmful to skin,samarium-cerium compounds containing Sm_(2)O_(2)S were synthesized by co-precipitation method.This kind of compounds blocks not only UV light,but also blue light.The minimum values of average transmittance(360-450 nm)and band gap of samarium-cerium compounds were 8.90%and 2.76 eV,respectively,which were less than 13.96%and 3.01 eV of CeO_(2).Elemental analysis(EA),X-ray diffraction(XRD),Fourier transformation infrared(FTIR),and Raman spectra determined that the samples contained Ce_(4)O_(7),Sm_(2)O_(2)S,Sm_(2)O_(3),and Sm_(2)O_(2)SO_(4).The microstructure of samples was analyzed by scanning and transmission electron microscopies(SEM and TEM).X-ray photoelectron spectrum(XPS)showed that cerium had Ce^(3+)and Ce^(4+) valence states,and oxygen was divided into lattice oxygen and oxygen vacancy,which was the direct cause of the decrease of average transmittance and band gap.

LSM12 facilitates the progression of colorectal cancer by activating the WNT/CTNNB1 signaling pathway

Aberrant activation of the WNT signaling pathway is a joint event in colorectal cancer(CRC),but the molecular mechanism is still unclear.Recently,RNA-splicing factor LSM12(like-Sm protein 12)is highly expressed in CRC tissues.This study aimed to verify whether LSM12 is involved in regulating CRC progression via regulating the WNT signaling pathway.Here,we found that LSM12 is highly expressed in CRC patient-derived tissues and cells.LSM12 is involved in the proliferation,invasion,and apoptosis of CRC cells,similar to the function of WNT signaling in CRC.Furthermore,protein interaction simulation and biochemical experiments proved that LSM12 directly binds to CTNNB1(also known asβ-Catenin)and regulates its protein stability to affect the CTTNB1-LEF1-TCF1 transcriptional complex formation and the associated WNT downstream signaling pathway.LSM12 depletion in CRC cells decreased the in vivo tumor growth through repression of cancer cell growth and acceleration of cancer cell apoptosis.Taken together,we suggest that the high expression of LSM12 is a novel factor leading to aberrant WNT signaling activation,and that strategies targeting this molecular mechanism may contribute to developing a new therapeutic method for CRC.

New perspectives on the genetic structure of dotted gizzard shad(Konosirus punctatus)based on RAD-seq

To maintain,develop and rationally utilize marine organisms,understanding their genetic structure and habitat adaptation pattern is necessary.Konosirus punctatus,which is a commercial fish species inhabiting the Indo-west Pacific Ocean,has shown an obvious annual global capture and aquaculture production decline due to climate changes and human activities.In the present study,restriction-site associated DNA sequencing(RAD-seq)was used to describe its genome-wide single nucleotide polymorphisms panel(SNPs).Among 146 individuals collected at nine locations scattered in China,Korea and Japan,a set of 632,090 SNPs were identified.Population genetic analysis showed that K.punctatus individuals were divided into two significant genetic clusters.Meanwhile,potential genetic differentiation between northern and southern population of K.punctatus was found.Treemix results indicated that gene flow existed among sampling locations of K.punctatus,especially from southern Japan to others.Moreover,candidate genes associated with habitat adaptations of K.punctatus were identified,which are involved in diverse physiological processes of K.punctatus including growth and development(e.g.,KIDINS220,PAN3),substance metabolism(e.g.,PGM5)and immune response(e.g.,VAV3,CCT7,HSPA12B).Our findings may aid in understanding the possible mechanisms for the population genetic structure and local adaptation of K.punctatus,which is beneficial to establish the management and conservation units of K.punctatus,guiding the rational use of resources,with reference significance for a profound understanding of the adaptative mechanisms of other marine organisms to the environment.

一例家族性低尿钙性高钙血症1型的临床特点及分子遗传学研究

报道1例家族性低尿钙性高钙血症1型(familial hypocalciuric hypercalcemia type 1,FHH1)患者的临床表现、遗传特点及诊治经过。患者反复发作胰腺炎伴中度高钙血症(最高3.22 mmol/L)及低尿钙,钙敏感受体(calcium-sensing receptor,CaSR)基因第2393位核苷酸C杂合突变为T,对应第798位氨基酸由脯氨酸变异为亮氨酸(c.2393C>T,p.P798L)。患者应用西那卡塞治疗后血钙及甲状旁腺激素水平较前显著下降。

Paleogene integrative stratigraphy and timescale of China

The Paleogene is the first period after the Mesozoic Mass Extinction. Mammals become the dominant group in the terrestrial ecosystem with a rapid radiation, and Asia has been considered to be the origin place of several mammalian groups.The Paleogene System consists mostly of terrestrial deposits in Asia, especially in East Asia. A well-established regional chronostratigraphic framework is the foundation for understanding both the Paleogene geologic history and evolutionary history of Asia and their relationships. The Paleogene is subdivided into the Paleocene, Eocene and Oligocene in the International Chronostratigraphic Chart. Based on the land mammal ages, the Chinese terrestrial Paleogene can be subdivided into 11 stages:the Shanghuan, Nongshanian and Bayanulanian stages of the Paleocene, the Lingchan, Arshantan, Irdinmanhan, Sharamurunian,Ulangochuian and Baiyinian stages of the Eocene, and the Ulantatalian and Tabenbulukian stages of the Oligocene. These stages have distinctive paleontological characters, with special significance of fossil mammals, which provide a reliable practical basis.The bases of the Shanghuan, Lingchan, and Ulantatalian stages are coincident respectively with those of the Paleocene, Eocene and Oligocene. The ages for their bases are determined as 66.0, 56.0 and 33.9 Ma, respectively, following that for the corresponding series in the International Chronostratigraphic Chart. For other stages, estimated ages are provided based on available paleomagnetic results.