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1.
PLoS One ; 19(5): e0303467, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-38820333

RESUMEN

In the investigation of stratigraphic reservoirs, a significant discrepancy frequently exists between the delineation of the formation pinch-out line as traced using the characteristics of seismic wave reflections and the actual location of the formation pinch-out line. This has been the main problem restricting further hydrocarbon exploration and development. In this study, Hala'alate Mountain on the northwestern margin of the Junggar Basin is taken as an example for carrying out the study of stratigraphic reservoirs by integrating logging, drilling, and 3D seismic data. On the one hand, in studies based on the identification of formation pinch-out points using seismic data, the identification error of reservoir pinch-out lines is reduced by the improved included angle extrapolation method by utilizing the half energy attribute. On the other hand, the Poisson's ratio curve is reconstructed using acoustic curves and oil-gas sensitive logging, then the reservoir oil-bearing facies zone is predicted using Poisson's ratio post-stack genetic inversion to comprehensively analyze the controlling factors of stratigraphic reservoirs. The study area mainly features structural lithologic reservoirs, structural stratigraphic reservoirs and stratigraphic overlaps that pinch out reservoirs. The boundary of a stratigraphic reservoir is affected by the dip angle of the unconformity surface, the formation dip angle, and other factors. The improved included angle extrapolation method improves the identification accuracy of stratigraphic overlap pinch-out reservoirs. The reservoir distribution then is calculated according to Poisson's ratio inversion, improving the prediction accuracy for the reservoir. This method improves the predictive effect for stratigraphic reservoirs and provides a new idea for the exploration and development of similar reservoirs.

2.
Heliyon ; 10(5): e26584, 2024 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-38463875

RESUMEN

A nearshore terminal fan is a special water system formed in arid environments. The characterisation of its thin-channel sand bodies has long been a challenge restricting oil and gas exploration. This study takes the Suning area of the Raoyang Sag as an example and uses the principles of seismic sedimentology to conduct seismic sedimentary research on the nearshore terminal fan of the first member of the Palaeogene Shahejie Formation (Es1) based on three-dimensional seismic, logging, and core analysis. Seven fourth-order sequences (SQV7) were identified within Es1, deposited by a fluvial river system terminating at the contracting bank of a lake. Prograding terminal fan sedimentary facies on a gentle slope zone were observed in the root mean square seismic attributes after spectral decomposition. We have successfully resolved the sandstone within the studied terminal fan system using a 90° phase conversion of the seismic data and red-green-blue (RGB) fusion of the various seismic attributes. The upper subsegment of the Shahejie Formation developed extensive nearshore terminal fan sedimentation, and the seismic sedimentological response characteristics were mainly channel-like and strip-shaped geomorphic systems deposited on gentle slope zones, indicating distributary channels and distal basin sedimentation. This study enriches our understanding of nearshore fans and provides ideas for predicting favourable sand bodies in this type of sedimentary facies.

3.
Sci Rep ; 14(1): 2448, 2024 01 30.
Artículo en Inglés | MEDLINE | ID: mdl-38291092

RESUMEN

In China, there has been a persistent upward trend in the incidence and mortality rates of colorectal cancer (CRC), with CRC ranking second in incidence and fifth in mortality among all malignant tumors. Although circular RNAs (circRNAs) have been implicated in the progression of various cancers, their specific role in CRC progression remains largely unexplored. The objective of this study was to elucidate the role and underlying mechanisms of circXRN2 in CRC. Differential expression of circXRN2 was identified through whole transcriptome sequencing. The expression levels of circXRN2 and miR-149-5p were quantified in CRC tissues, corresponding adjacent normal tissues, and CRC cell lines using quantitative reverse transcription-polymerase chain reaction (qRT-PCR). The stability of circXRN2 was confirmed through RNase R and actinomycin D experiments. The binding interaction between circXRN2 and miR-149-5p was validated through RNA pull-down, RNA immunoprecipitation, and dual-luciferase assays. The biological functions of circXRN2 were assessed through a battery of in vitro experiments, including the CCK-8 assay, EdU assay, scratch assay, Transwell assay, and flow cytometry assay. Additionally, in vivo experiments involving a tumor transplantation model and a liver-lung metastasis model were conducted. The influence of circXRN2 on the expression of epithelial-mesenchymal transition (EMT)-related genes was determined via Western blotting analysis. In CRC tissues and cells, there was an upregulation in the expression levels of both circXRN2 and ENC1, while miR-149-5p exhibited a downregulation in its expression. The overexpression of circXRN2 was found to enhance tumor proliferation and metastasis, as evidenced by results from both in vitro and in vivo experiments. Functionally, circXRN2 exerted its antitumor effect by suppressing cell proliferation, migration, and invasion while also promoting apoptosis. Mechanistically, the dysregulated expression of circXRN2 had an impact on the expression of proteins within the EMT signaling pathway. Our results demonstrated that circXRN2 promoted the proliferation and metastasis of CRC cells through the miR-149-5p/ENC1/EMT axis, suggesting that circXRN2 might serve as a potential therapeutic target and novel biomarker in the progression of CRC.


Asunto(s)
Neoplasias Colorrectales , Neoplasias Hepáticas , Neoplasias Pulmonares , MicroARNs , Humanos , MicroARNs/metabolismo , Neoplasias Colorrectales/patología , Línea Celular , Neoplasias Pulmonares/genética , Neoplasias Hepáticas/genética , Transición Epitelial-Mesenquimal/genética , Proliferación Celular/genética , Línea Celular Tumoral , Regulación Neoplásica de la Expresión Génica , Transactivadores/metabolismo
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