Weakly-Supervised Dense Video Captioning (WSDVC) aims to localize and describe all events of interest in a video without requiring annotations of event boundaries. This setting poses a great challenge in accurately locating the temporal location of event, as the relevant supervision is unavailable. Existing methods rely on explicit alignment constraints between event locations and captions, which involve complex event proposal procedures during both training and inference. To tackle this problem, we propose a novel implicit location-caption alignment paradigm by complementary masking, which simplifies the complex event proposal and localization process while maintaining effectiveness. Specifically, our model comprises two components: a dual-mode video captioning module and a mask generation module. The dual-mode video captioning module captures global event information and generates descriptive captions, while the mask generation module generates differentiable positive and negative masks for localizing the events. These masks enable the implicit alignment of event locations and captions by ensuring that captions generated from positively and negatively masked videos are complementary, thereby forming a complete video description. In this way, even under weak supervision, the event location and event caption can be aligned implicitly. Extensive experiments on the public datasets demonstrate that our method outperforms existing weakly-supervised methods and achieves competitive results compared to fully-supervised methods.

We know that different types of cancers usually have different responses to the same treatment. Therefore, it is important to understand the similarities and differences across subtypes of cancers, so as to provide a basis for the individualized treatments. Until now, no comprehensive investigation on competing endogenous RNAs (ceRNAs) has been reported for the three main subtypes of renal cell carcinoma (RCC), so the regulation characteristics of ceRNAs in three subtypes are not well revealed. This paper firstly describes a comparative analysis of ceRNA-ceRNA interaction networks for all the three subtypes of RCC based on differential microRNAs (miRNAs). We comprehensively summarized all miRNA and messenger RNAdata of RCC from 126 matched tumor-normal tissues in The Cancer Genome Atlas, systematically analyzed a total of more than 80 000 ceRNA interactions and highlighted the common and specific properties among them, aiming to identify critical genes to classify them for providing supplementary help in the precise diagnosis of RCC. From three aspects, including common or specific ceRNAs, upregulated or downregulated and classifications across the three subtypes, we highlighted the common and specific properties for the three subtypes and also explored the classification of RCC by combining the specific ceRNAs with differential regulations. Moreover, for the most major subtype of clear cell renal cell carcinoma (KIRC), three critical genes were screened out from KIRC ceRNA network and further demonstrated to be the potential biomarkers of KIRC by performing biological experiments at the transcriptional level.