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An ideal animal model is a prerequisite for the basic research of uterus transplantation. This study aimed to develop a new cervical ectopic uterus transplantation mice model, which was established by vascular anastomosis of the right common iliac artery and vein of the donor with the right common carotid artery and external jugular vein of the recipient, respectively, using the cuff method. The survival status of the transplanted uterus was assessed by macroscopic observation and histological examination after surgery, and the function of the graft uterus was tested by verifying whether the pregnancy is possible. A total of 40 transplants were performed, of which only 1 failed due to donor hemorrhage. After 26 transplants, the total operation time reduced to 52.4 ± 3.8 minutes, of which the total ischemia time took 6.6 ± 1.1 minutes. Sixty days after transplantation, all the graft uteri had a good blood supply and spontaneous contraction. The histology showed no significant difference between the transplanted uterus and the native. Embryo transfer experiments have proven that the transplanted uterus has uterine function. In conclusion, this new model is an effective and simple mice model for the studies of the scientific issues related to uterus transplantation.
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Nascido Vivo , Transplantes , Animais , Feminino , Humanos , Artéria Ilíaca , Camundongos , Gravidez , Doadores de Tecidos , Útero/transplanteRESUMO
We address the problem of lung CT image registration, which underpins various diagnoses and treatments for lung diseases. The main crux of the problem is the large deformation that the lungs undergo during respiration. This physiological process imposes several challenges from a learning point of view. In this paper, we propose a novel training scheme, called stochastic decomposition, which enables deep networks to effectively learn such a difficult deformation field during lung CT image registration. The key idea is to stochastically decompose the deformation field, and supervise the registration by synthetic data that have the corresponding appearance discrepancy. The stochastic decomposition allows for revealing all possible decompositions of the deformation field. At the learning level, these decompositions can be seen as a prior to reduce the ill-posedness of the registration yielding to boost the performance. We demonstrate the effectiveness of our framework on Lung CT data. We show, through extensive numerical and visual results, that our technique outperforms existing methods.
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Processos Estocásticos , Tomografia Computadorizada por Raios X , Tomografia Computadorizada por Raios X/métodos , Humanos , Interpretação de Imagem Radiográfica Assistida por Computador/métodos , Pulmão/diagnóstico por imagem , Algoritmos , Pneumopatias/diagnóstico por imagem , Pneumopatias/fisiopatologiaRESUMO
Segmenting overlapping cytoplasms in cervical smear images is a clinically essential task for quantitatively measuring cell-level features to screen cervical cancer This task, however, remains rather challenging, mainly due to the deficiency of intensity (or color) information in the overlapping region Although shape prior-based models that compensate intensity deficiency by introducing prior shape information about cytoplasm are firmly established, they often yield visually implausible results, as they model shape priors only by limited shape hypotheses about cytoplasm, exploit cytoplasm-level shape priors alone, and impose no shape constraint on the resulting shape of the cytoplasm In this paper, we present an effective shape prior-based approach, called constrained multi-shape evolution, that segments all overlapping cytoplasms in the clump simultaneously by jointly evolving each cytoplasm's shape guided by the modeled shape priors We model local shape priors (cytoplasm-level) by an infinitely large shape hypothesis set which contains all possible shapes of the cytoplasm In the shape evolution, we compensate intensity deficiency for the segmentation by introducing not only the modeled local shape priors but also global shape priors (clump-level) modeled by considering mutual shape constraints of cytoplasms in the clump We also constrain the resulting shape in each evolution to be in the built shape hypothesis set for further reducing implausible segmentation results We evaluated the proposed method in two typical cervical smear datasets, and the extensive experimental results confirm its effectiveness.
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Algoritmos , Teste de Papanicolaou , Neoplasias do Colo do Útero , Feminino , Humanos , Citoplasma/patologia , Detecção Precoce de Câncer , Teste de Papanicolaou/métodos , Neoplasias do Colo do Útero/diagnósticoRESUMO
Cell classification underpins intelligent cervical cancer screening, a cytology examination that effectively decreases both the morbidity and mortality of cervical cancer. This task, however, is rather challenging, mainly due to the difficulty of collecting a training dataset representative sufficiently of the unseen test data, as there are wide variations of cells' appearance and shape at different cancerous statuses. This difficulty makes the classifier, though trained properly, often classify wrongly for cells that are underrepresented by the training dataset, eventually leading to a wrong screening result. To address it, we propose a new learning algorithm, called worse-case boosting, for classifiers effectively learning from under-representative datasets in cervical cell classification. The key idea is to learn more from worse-case data for which the classifier has a larger gradient norm compared to other training data, so these data are more likely to correspond to underrepresented data, by dynamically assigning them more training iterations and larger loss weights for boosting the generalizability of the classifier on underrepresented data. We achieve this idea by sampling worse-case data per the gradient norm information and then enhancing their loss values to update the classifier. We demonstrate the effectiveness of this new learning algorithm on two publicly available cervical cell classification datasets (the two largest ones to the best of our knowledge), and positive results (4% accuracy improvement) yield in the extensive experiments. The source codes are available at: https://github.com/YouyiSong/Worse-Case-Boosting.
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Neoplasias do Colo do Útero , Feminino , Humanos , Detecção Precoce de Câncer , Algoritmos , SoftwareRESUMO
Ovarian cancer (OvCa) is characterized by early metastasis and high mortality rates, underscoring the need for deeper understanding of these aspects. This study explores the role of glucose transporter 3 (GLUT3) driven by zinc finger E-box-binding homeobox 1 (ZEB1) in OvCa progression and metastasis. Specifically, this study explored whether ZEB1 promotes glycolysis and assessed the potential involvement of GLUT3 in this process in OvCa cells. Our findings revealed that ZEB1 and GLUT3 were excessively expressed and closely correlated in OvCa. Mechanistically, ZEB1 activates the transcription of GLUT3 by binding to its promoter region. Increased expression of GLUT3 driven by ZEB1 dramatically enhances glycolysis, and thus fuels Warburg Effect to promote OvCa progression and metastasis. Consistently, elevated ZEB1 and GLUT3 expression in clinical OvCa is correlated with poor prognosis, reinforcing the profound contribution of ZEB1-GLUT3 axis to OvCa. These results suggest that activation of GLUT3 expression by ZEB1 is crucial for the proliferation and metastasis of OvCa via fueling glycolysis, shedding new light on OvCa treatment.
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Progressão da Doença , Regulação Neoplásica da Expressão Gênica , Transportador de Glucose Tipo 3 , Neoplasias Ovarianas , Ativação Transcricional , Efeito Warburg em Oncologia , Homeobox 1 de Ligação a E-box em Dedo de Zinco , Humanos , Homeobox 1 de Ligação a E-box em Dedo de Zinco/genética , Homeobox 1 de Ligação a E-box em Dedo de Zinco/metabolismo , Transportador de Glucose Tipo 3/genética , Transportador de Glucose Tipo 3/metabolismo , Feminino , Neoplasias Ovarianas/genética , Neoplasias Ovarianas/patologia , Neoplasias Ovarianas/metabolismo , Linhagem Celular Tumoral , Glicólise/genética , Animais , Proliferação de Células/genética , Camundongos , Regiões Promotoras Genéticas , Camundongos NusRESUMO
Deep neural networks often suffer from performance inconsistency for multiorgan segmentation in medical images; some organs are segmented far worse than others. The main reason might be organs with different levels of learning difficulty for segmentation mapping, due to variations such as size, texture complexity, shape irregularity, and imaging quality. In this article, we propose a principled class-reweighting algorithm, termed dynamic loss weighting, which dynamically assigns a larger loss weight to organs if they are discriminated as more difficult to learn according to the data and network's status, for forcing the network to learn from them more to maximally promote the performance consistency. This new algorithm uses an extra autoencoder to measure the discrepancy between the segmentation network's output and the ground truth and dynamically estimates the loss weight of organs per the contribution of the organ to the new updated discrepancy. It can capture the variation in organs' learning difficult during training, and it is neither sensitive to data's property nor dependent on human priors. We evaluate this algorithm in two multiorgan segmentation tasks: abdominal organs and head-neck structures, on publicly available datasets, with positive results obtained from extensive experiments which confirm the validity and effectiveness. Source codes are available at: https://github.com/YouyiSong/Dynamic-Loss-Weighting.
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Detecting cells in blood smear images is of great significance for automatic diagnosis of blood diseases. However, this task is rather challenging, mainly because there are dense cells that are often overlapping, making some of the occluded boundary parts invisible. In this paper, we propose a generic and effective detection framework that exploits non-overlapping regions (NOR) for providing discriminative and confident information to compensate the intensity deficiency. In particular, we propose a feature masking (FM) to exploit the NOR mask generated from the original annotation information, which can guide the network to extract NOR features as supplementary information. Furthermore, we exploit NOR features to directly predict the NOR bounding boxes (NOR BBoxes). NOR BBoxes are combined with the original BBoxes for generating one-to-one corresponding BBox-pairs that are used for further improving the detection performance. Different from the non-maximum suppression (NMS), our proposed non-overlapping regions NMS (NOR-NMS) uses the NOR BBoxes in the BBox-pairs to calculate intersection over union (IoU) for suppressing redundant BBoxes, and consequently retains the corresponding original BBoxes, circumventing the dilemma of NMS. We conducted extensive experiments on two publicly available datasets, with positive results demonstrating the effectiveness of the proposed method against existing methods.
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Collecting sufficient high-quality training data for deep neural networks is often expensive or even unaffordable in medical image segmentation tasks. We thus propose to train the network by using external data that can be collected in a cheaper way, e.g., crowd-sourcing. We show that by data discernment, the network is able to mine valuable knowledge from external data, even though the data distribution is very different from that of the original (internal) data. We discern the external data by learning an importance weight for each of them, with the goal to enhance the contribution of informative external data to network updating, while suppressing the data that are 'useless' or even 'harmful'. An iterative algorithm that alternatively estimates the importance weight and updates the network is developed by formulating the data discernment as a constrained nonlinear programming problem. It estimates the importance weight according to the distribution discrepancy between the external data and the internal dataset, and imposes a constraint to drive the network to learn more effectively, compared with the network without using the external data. We evaluate the proposed algorithm on two tasks: abdominal CT image and cervical smear image segmentation, using totally 6 publicly available datasets. The effectiveness of the algorithm is demonstrated by extensive experiments. Source codes are available at: https://github.com/YouyiSong/Data-Discernment.
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Algoritmos , Crowdsourcing , Redes Neurais de Computação , Software , Processamento de Imagem Assistida por ComputadorRESUMO
Recently, federated learning has become a powerful technique for medical image classification due to its ability to utilize datasets from multiple clinical clients while satisfying privacy constraints. However, there are still some obstacles in federated learning. Firstly, most existing methods directly average the model parameters collected by medical clients on the server, ignoring the specificities of the local models. Secondly, class imbalance is a common issue in medical datasets. In this paper, to handle these two challenges, we propose a novel specificity-aware federated learning framework that benefits from an Adaptive Aggregation Mechanism (AdapAM) and a Dynamic Feature Fusion Strategy (DFFS). Considering the specificity of each local model, we set the AdapAM on the server. The AdapAM utilizes reinforcement learning to adaptively weight and aggregate the parameters of local models based on their data distribution and performance feedback for obtaining the global model parameters. For the class imbalance in local datasets, we propose the DFFS to dynamically fuse the features of majority classes based on the imbalance ratio in the min-batch and collaborate the rest of features. We conduct extensive experiments on a dermoscopic dataset and a fundus image dataset. Experimental results show that our method can achieve state-of-the-art results in these two real-world medical applications.
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The alignment of images through deformable image registration is vital to clinical applications (e.g., atlas creation, image fusion, and tumor targeting in image-guided navigation systems) and is still a challenging problem. Recent progress in the field of deep learning has significantly advanced the performance of medical image registration. In this review, we present a comprehensive survey on deep learning-based deformable medical image registration methods. These methods are classified into five categories: Deep Iterative Methods, Supervised Methods, Unsupervised Methods, Weakly Supervised Methods, and Latest Methods. A detailed review of each category is provided with discussions about contributions, tasks, and inadequacies. We also provide statistical analysis for the selected papers from the point of view of image modality, the region of interest (ROI), evaluation metrics, and method categories. In addition, we summarize 33 publicly available datasets that are used for benchmarking the registration algorithms. Finally, the remaining challenges, future directions, and potential trends are discussed in our review.
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Early diagnosis is currently the most effective way of saving the life of patients with neuropsychiatric systemic lupus erythematosus (NPSLE). However, it is rather difficult to detect this terrible disease at the early stage, due to the subtle and elusive symptomatic signals. Recent studies show that the 1H-MRS (proton magnetic resonance spectroscopy) imaging technique can capture more information reflecting the early appearance of this disease than conventional magnetic resonance imaging techniques. 1H-MRS data, however, also presents more noises that can bring serious diagnosis bias. We hence proposed a noise-immune extreme ensemble learning technique for effectively leveraging 1H-MRS data for advancing the early diagnosis of NPSLE. Our main results are that 1) by developing generalized maximum correntropy criterion in the kernel extreme learning setting, many types of non-Gaussian noises can be distinguished, and 2) weighted recursive feature elimination, using maximal information coefficient to weight feature's importance, helps to further alleviate the bad impact of noises on the diagnosis performance. The proposed method is assessed on a publicly available dataset with 97.5% accuracy, 95.8% sensitivity and 99.9% specificity, which well demonstrates its efficacy.
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Lúpus Eritematoso Sistêmico , Vasculite Associada ao Lúpus do Sistema Nervoso Central , Diagnóstico Precoce , Humanos , Lúpus Eritematoso Sistêmico/diagnóstico por imagem , Vasculite Associada ao Lúpus do Sistema Nervoso Central/diagnóstico por imagem , Aprendizado de Máquina , Imageamento por Ressonância Magnética/métodosRESUMO
In [1], Baiying Lei was indicated as the corresponding author. Tianfu Wang and Baiying Lei should have been indicated as the corresponding authors.
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We present a novel approach for segmenting overlapping cytoplasm of cells in cervical smear images by leveraging the adaptive shape priors extracted from cytoplasm's contour fragments and shape statistics. The main challenge of this task is that many occluded boundaries in cytoplasm clumps are extremely difficult to be identified and, sometimes, even visually indistinguishable. Given a clump where multiple cytoplasms overlap, our method starts by cutting its contour into a set of contour fragments. We then locate the corresponding contour fragments of each cytoplasm by a grouping process. For each cytoplasm, according to the grouped fragments and a set of known shape references, we construct its shape and, then, connect the fragments to form a closed contour as the segmentation result, which is explicitly constrained by the constructed shape. We further integrate the intensity and curvature information, which is complementary to the shape priors extracted from contour fragments, into our framework to improve the segmentation accuracy. We propose to iteratively conduct fragments grouping, shape constructing, and fragments connecting for progressively refining the shape priors and improving the segmentation results. We extensively evaluate the effectiveness of our method on two typical cervical smear datasets. The experimental results demonstrate that our approach is highly effective and consistently outperforms the state-of-the-art approaches. The proposed method is general enough to be applied to other similar microscopic image segmentation tasks, where heavily overlapped objects exist.
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Citoplasma/classificação , Detecção Precoce de Câncer/métodos , Interpretação de Imagem Assistida por Computador/métodos , Esfregaço Vaginal/métodos , Algoritmos , Feminino , Humanos , Redes Neurais de Computação , Neoplasias do Colo do Útero/diagnóstico por imagemRESUMO
Objective To evaluate the associations between dietary fiber intake and ovarian cancer risk. Methods A literature survey was conducted by searching the PubMed, Web of Science, and Wanfang Med Online databases up to March 1st, 2018. The effect of dietary fiber intake on ovarian cancer risk was evaluated by calculating relative risks with 95% confidence intervals (95%CI) using Stata 12.0 software. Results A total of 17 articles with 149,177 participants including 7609 ovarian cancer patients were included in this analysis. The summarized relative risk for ovarian cancer in participants with the highest compared with the lowest fiber intake was 0.760 (95%CI=0.702-0.823), with no significant between-study heterogeneity ( I2=12.4%). Subgroup analysis according to study design demonstrated positive associations in both cohort studies and case-control studies. Moreover, the results were consistent among populations from America, Europe, and Asia. No publication bias was found by Egger's test or funnel plots. Conclusion This meta-analysis concluded that a high intake of dietary fiber could significantly reduce the risk of ovarian cancer compared with a low fiber intake.
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Fibras na Dieta/estatística & dados numéricos , Neoplasias Ovarianas/epidemiologia , Ásia/epidemiologia , Intervalos de Confiança , Dieta/estatística & dados numéricos , Ingestão de Alimentos , Europa (Continente)/epidemiologia , Feminino , Humanos , Estudos Observacionais como Assunto , Risco , Estados Unidos/epidemiologiaRESUMO
Estrogenic signals have been suggested to be important for the tumorigenesis and progression of endometrial cancer (EC) cells. Our present data showed that estrogen related receptor alpha (ERRα), while not ERRß or ERRγ, was significantly elevated in EC cells and tissues when compared to their controls. Targeted inhibition of ERRα by siRNA or its inverse agonist XCT-790 can suppress the migration and invasion of EC cells. Both si-ERRα and XCT-790 decreased the expression of transforming growth factor-beta (TGF-ß). ERRα can directly bind with the promoter of TGFB1 and then increase its transcription. Further, ERRα was involved in the positive self-feedback loop of TGF-ß in EC cells. Targeted inhibition of ERRα/TGF-ß can synergistically suppress the in vitro invasion of EC cells. Collectively, our data suggested that ERRα can trigger the cell migration and invasion via increasing the positive self-feedback regulation of TGF-ß.
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Movimento Celular/fisiologia , Neoplasias do Endométrio/metabolismo , Estrogênios/metabolismo , Receptores de Estrogênio/metabolismo , Fator de Crescimento Transformador beta1/metabolismo , Proliferação de Células/fisiologia , Neoplasias do Endométrio/patologia , Feminino , Humanos , Receptor ERRalfa Relacionado ao EstrogênioRESUMO
Quantitative analysis of bacterial morphotypes in the microscope images plays a vital role in diagnosis of bacterial vaginosis (BV) based on the Nugent score criterion. However, there are two main challenges for this task: 1) It is quite difficult to identify the bacterial regions due to various appearance, faint boundaries, heterogeneous shapes, low contrast with the background, and small bacteria sizes with regards to the image. 2) There are numerous bacteria overlapping each other, which hinder us to conduct accurate analysis on individual bacterium. To overcome these challenges, we propose an automatic method in this paper to diagnose BV by quantitative analysis of bacterial morphotypes, which consists of a three-step approach, i.e., bacteria regions segmentation, overlapping bacteria splitting, and bacterial morphotypes classification. Specifically, we first segment the bacteria regions via saliency cut, which simultaneously evaluates the global contrast and spatial weighted coherence. And then Markov random field model is applied for high-quality unsupervised segmentation of small object. We then decompose overlapping bacteria clumps into markers, and associate a pixel with markers to identify evidence for eventual individual bacterium splitting. Next, we extract morphotype features from each bacterium to learn the descriptors and to characterize the types of bacteria using an Adaptive Boosting machine learning framework. Finally, BV diagnosis is implemented based on the Nugent score criterion. Experiments demonstrate that our proposed method achieves high accuracy and efficiency in computation for BV diagnosis.
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Bactérias/citologia , Interpretação de Imagem Assistida por Computador/métodos , Microscopia/métodos , Vaginose Bacteriana/diagnóstico por imagem , Adolescente , Adulto , Algoritmos , Feminino , Humanos , Pessoa de Meia-Idade , Adulto JovemRESUMO
Accurate segmentation of cervical cells in Pap smear images is an important step in automatic pre-cancer identification in the uterine cervix. One of the major segmentation challenges is overlapping of cytoplasm, which has not been well-addressed in previous studies. To tackle the overlapping issue, this paper proposes a learning-based method with robust shape priors to segment individual cell in Pap smear images to support automatic monitoring of changes in cells, which is a vital prerequisite of early detection of cervical cancer. We define this splitting problem as a discrete labeling task for multiple cells with a suitable cost function. The labeling results are then fed into our dynamic multi-template deformation model for further boundary refinement. Multi-scale deep convolutional networks are adopted to learn the diverse cell appearance features. We also incorporated high-level shape information to guide segmentation where cell boundary might be weak or lost due to cell overlapping. An evaluation carried out using two different datasets demonstrates the superiority of our proposed method over the state-of-the-art methods in terms of segmentation accuracy.
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Teste de Papanicolaou , Algoritmos , Feminino , Humanos , Neoplasias do Colo do ÚteroRESUMO
In this paper, a multiscale convolutional network (MSCN) and graph-partitioning-based method is proposed for accurate segmentation of cervical cytoplasm and nuclei. Specifically, deep learning via the MSCN is explored to extract scale invariant features, and then, segment regions centered at each pixel. The coarse segmentation is refined by an automated graph partitioning method based on the pretrained feature. The texture, shape, and contextual information of the target objects are learned to localize the appearance of distinctive boundary, which is also explored to generate markers to split the touching nuclei. For further refinement of the segmentation, a coarse-to-fine nucleus segmentation framework is developed. The computational complexity of the segmentation is reduced by using superpixel instead of raw pixels. Extensive experimental results demonstrate that the proposed cervical nucleus cell segmentation delivers promising results and outperforms existing methods.
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Núcleo Celular/química , Colo do Útero/citologia , Citoplasma/química , Processamento de Imagem Assistida por Computador/métodos , Colo do Útero/patologia , Feminino , Histocitoquímica , Humanos , MicroscopiaRESUMO
In this paper, a superpixel and convolution neural network (CNN) based segmentation method is proposed for cervical cancer cell segmentation. Since the background and cytoplasm contrast is not relatively obvious, cytoplasm segmentation is first performed. Deep learning based on CNN is explored for region of interest detection. A coarse-to-fine nucleus segmentation for cervical cancer cell segmentation and further refinement is also developed. Experimental results show that an accuracy of 94.50% is achieved for nucleus region detection and a precision of 0.9143±0.0202 and a recall of 0.8726±0.0008 are achieved for nucleus cell segmentation. Furthermore, our comparative analysis also shows that the proposed method outperforms the related methods.