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Wiley

SCOPUS (SonsInc.)SCIE-ISI

  2523-3548

  2523-3548

 

Cơ quản chủ quản:  WILEY , John Wiley & Sons Inc.

Lĩnh vực:
OncologyCancer Research

Các bài báo tiêu biểu

Global patterns of breast cancer incidence and mortality: A population‐based cancer registry data analysis from 2000 to 2020
Tập 41 Số 11 - Trang 1183-1194 - 2021
Shaoyuan Lei, Rongshou Zheng, Siwei Zhang, Shaoming Wang, Ru Chen, Kexin Sun, Hongmei Zeng, Jiachen Zhou, Wenqiang Wei
AbstractBackground

Breast cancer is the most commonly diagnosed cancer and leading cause of cancer death among women worldwide but has patterns and trends which vary in different countries. This study aimed to evaluate the global patterns of breast cancer incidence and mortality and analyze its temporal trends for breast cancer prevention and control.

Methods

Breast cancer incidence and mortality data in 2020 were obtained from the GLOBOCAN online database. Continued data from the Cancer Incidence in Five Continents Time Trends, the International Agency for Research on cancer mortality and China National Central Cancer Registry were used to analyze the time trends from 2000 to 2015 through Joinpoint regression, and annual average percent changes of breast cancer incidence and mortality were calculated. Association between Human Development Index and breast cancer incidence and mortality were estimated by linear regression.

Results

There were approximately 2.3 million new breast cancer cases and 685,000 breast cancer deaths worldwide in 2020. Its incidence and mortality varied among countries, with the age‐standardized incidence ranging from the highest of 112.3 per 100,000 population in Belgium to the lowest of 35.8 per 100,000 population in Iran, and the age‐standardized mortality from the highest of 41.0 per 100,000 population in Fiji to the lowest of 6.4 per 100,000 population in South Korea. The peak age of breast cancer in some Asian and African countries were over 10 years earlier than in European or American countries. As for the trends of breast cancer, the age‐standardized incidence rates significantly increased in China and South Korea but decreased in the United States of America (USA) during 2000‐2012. Meanwhile, the age‐standardized mortality rates significantly increased in China and South Korea but decreased in the United Kingdom, the USA, and Australia during 2000 and 2015.

Conclusions

The global burden of breast cancer is rising fast and varies greatly among countries. The incidence and mortality rates of breast cancer increased rapidly in China and South Korea but decreased in the USA. Increased health awareness, effective prevention strategies, and improved access to medical treatment are extremely important to curb the snowballing breast cancer burden, especially in the most affected countries.

Cancer burden of major cancers in China: A need for sustainable actions
Tập 40 Số 5 - Trang 205-210 - 2020
Maomao Cao, Li He, Dianqin Sun, Wanqing Chen
Abstract

Cancer is still a major health problem in China although numerous efforts have been made for its prevention and control. Findings from this study showed that lung cancer remains the most common type of cancer diagnosed, and was attributed to nearly 30% of all cancer‐related deaths. The incidence of the five most common cancers, in China, in 2015, including cancers of the lungs, stomach, colorectum, liver and breast, accounted for almost 60% of all cancers diagnosed. The high cancer burden in China highlights the need for further improvement in health education, professional training and the building up an anti‐cancer network for introducing and implementing sustainable actions for cancer control.

Mucinous colorectal adenocarcinoma: clinical pathology and treatment options
Tập 39 Số 1 - Trang 1-13 - 2019
Cong Luo, Shuyi Cen, Guojun Ding, Wei Wang
Abstract

Mucinous colorectal adenocarcinoma is a distinct subtype of colorectal cancer (CRC) characterized by the presence of abundant extracellular mucin which accounts for at least 50% of the tumor volume. Mucinous colorectal adenocarcinoma is found in 10%–20% of CRC patients and occurs more commonly in female and younger patients. Moreover, mucinous colorectal adenocarcinoma is more frequently located in the proximal colon and diagnosed at an advanced stage. Based on its molecular context, mucinous colorectal adenocarcinoma is associated with the overexpression of mucin 2 (MUC2) and mucin 5AC (MUC5AC) proteins. At the same time, it shows higher mutation rates in the fundamental genes of the RAS/MAPK and PI3K/Akt/mTOR pathways. Mucinous colorectal adenocarcinoma also shows higher rates of microsatellite instability (MSI) than non‐mucinous colorectal adenocarcinoma which might correlate it with Lynch syndrome and the CpG island methylator phenotype. The prognosis of mucinous colorectal adenocarcinoma as to non‐mucinous colorectal adenocarcinoma is debatable. Further, the impaired responses of mucinous colorectal adenocarcinoma to palliative or adjuvant chemotherapy warrant more studies to be performed for a specialized treatment for these patients. In this review, we discuss the molecular background and histopathology of mucinous colorectal adenocarcinoma, and provide an update on its prognosis and therapeutics from recent literatures.

Impaired dendritic cell functions in lung cancer: a review of recent advances and future perspectives
- 2019
Jingbo Wang, Xue F. Huang, Furong Li
Abstract

Lung cancer is the leading cause of cancer mortality worldwide. Dendritic cells (DCs) are the key factors providing protective immunity against lung tumors and clinical trials have proven that DC function is reduced in lung cancer patients. It is evident that the immunoregulatory network may play a key role in the failure of the immune response to terminate tumors. Lung tumors likely employ numerous strategies to suppress DC‐based anti‐tumor immunity. Here, we summarize the recent advances in our understanding on lung tumor‐induced immunosuppression in DCs, which affects the initiation and development of T‐cell responses. We also describe which existing measures to restore DC function may be useful for clinical treatment of lung tumors. Furthering our knowledge of how lung cancer cells alter DC function to generate a tumor‐supportive environment will be essential in order to guide the design of new immunotherapy strategies for clinical use.

Độc tính tim mạch của 5‐fluorouracil và capecitabine ở bệnh nhân Trung Quốc: một nghiên cứu triển vọng Dịch bởi AI
Tập 38 Số 1 - Trang 1-7 - 2018
Jianjun Peng, Chao Dong, Chang Wang, Weihua Li, Hui Yu, Min Zhang, Qun Zhao, Bo Zhu, Jun Zhang, Wenliang Li, Fenghua Wang, Qiong Wu, Wenhao Zhou, Ying Yuan, Meng Qiu, Gong Chen
Tóm tắtGiới thiệu

Độc tính tim mạch liên quan đến 5‐fluorouracil (5‐FU) và capecitabine, từ các bất thường điện tâm đồ không có triệu chứng cho đến nhồi máu cơ tim nghiêm trọng, đã được báo cáo trong một số nghiên cứu. Tuy nhiên, tình trạng độc tính tim mạch này ở bệnh nhân Trung Quốc có bệnh ác tính vẫn chưa được điều tra đến nay. Trong nghiên cứu hiện tại, chúng tôi nhằm đánh giá một cách triển vọng tỷ lệ xảy ra và các biểu hiện lâm sàng của độc tính tim mạch liên quan đến 5‐FU và capecitabine ở bệnh nhân ung thư được tuyển chọn từ nhiều trung tâm tại Trung Quốc.

Phương pháp

Trong số 527 bệnh nhân hoàn thành nghiên cứu, 196 người được điều trị hóa chất dựa trên 5‐FU và 331 người được điều trị hóa chất dựa trên capecitabine với tư cách là liệu pháp đầu tay hoặc bổ trợ. Các biến cố bất lợi đã được báo cáo trong suốt quá trình điều trị và lên đến 28 ngày theo dõi. Các chỉ số kết quả bao gồm điện tâm đồ (ECG), enzyme cơ tim, troponin tim, peptide natri lợi niệu và siêu âm tim. Phân tích đơn biến và hồi quy logistic đã được tiến hành để phân tích theo nhóm và xác định các biến số độc lập có ý nghĩa liên quan đến độc tính tim mạch của cả hai loại thuốc này.

Kết quả

Tổng cộng, 161 trên 527 bệnh nhân (30.6%) trải qua độc tính tim mạch. Tỷ lệ xảy ra của độc tính tim mạch là 33.8% (112/331) trong nhóm capecitabine, cao hơn đáng kể so với tỷ lệ 25% (49/196) trong nhóm 5‐FU (P = 0.0042). 110/527 bệnh nhân (20.9%) gặp phải rối loạn nhịp tim, 105/527 (19.9%) phát triển các thay đổi thiếu máu cục bộ, trong khi chỉ 20/527 bệnh nhân (3.8%) biểu hiện suy tim và 6/527 bệnh nhân (1.1%) có nhồi máu cơ tim. Các bệnh lý tim mạch hiện có, tăng huyết áp, hóa trị liệu dựa trên capecitabine và thời gian điều trị đã được xác định là các yếu tố nguy cơ quan trọng liên quan đến độc tính tim mạch. Tỷ lệ odds lần lượt là 15.7 (tiền sử bệnh tim so với không có tiền sử), 1.86 (capecitabine so với 5‐FU), 1.06 (5–8 chu kỳ hóa trị so với 1–4 chu kỳ) và 1.58 (tăng huyết áp so với không tăng huyết áp).

Kết luận

Độc tính tim mạch do fluoropyrimidine gây ra trong dân số Trung Quốc có thể bị đánh giá thấp trong thực hành lâm sàng. Việc theo dõi chặt chẽ bệnh nhân được khuyến nghị, đặc biệt là đối với những bệnh nhân có nguy cơ cao về độc tính tim mạch. Các yếu tố nguy cơ có thể bao gồm thời gian điều trị, hóa trị liệu dựa trên capecitabine, các bệnh tim mạch hiện có và tăng huyết áp.

Đăng ký thử nghiệm Nghiên cứu này được bắt đầu vào ngày 22 tháng 1 năm 2014 và đã được đăng ký hồi cứu với số đăng ký ChiCTR1800015434

Laparoscopic versus open pancreaticoduodenectomy for pancreatic ductal adenocarcinoma: a propensity score matching analysis
- 2019
Wentao Zhou, Weiwei Jin, Dansong Wang, Chao Lü, Xuefeng Xu, Ren-Chao Zhang, Tiantao Kuang, Yucheng Zhou, Wen-Chuan Wu, Dayong Jin, Yiping Mou, Wenhui Lou
AbstractBackground

A growing body of evidence supports the use of laparoscopic pancreaticoduodenectomy (LPD) as an efficient and feasible surgical technique. However, few studies have investigated its applicability in pancreatic ductal adenocarcinoma (PDAC), and the long‐term efficacy of LPD on PDAC remains unclear. This study aimed to compare the short‐ and long‐term outcomes between LPD and open pancreaticoduodenectomy (OPD) for PDAC.

Methods

The data of patients who had OPD or LPD for PDAC between January 2013 and September 2017 were retrieved. Their postoperative outcomes and survival were compared after propensity score matching.

Results

A total of 309 patients were included. After a 2:1 matching, 93 cases in the OPD group and 55 in the LPD group were identified. Delayed gastric emptying (DGE), particularly grade B/C DGE, occurred less frequently in the LPD group than in the OPD group (1.8% vs. 36.6%, P < 0.001; 1.8% vs. 22.6%, P = 0.001). The overall complication rates were significantly lower in the LPD group than in the OPD group (49.1% vs. 71.0%, P = 0.008), whereas the rates of major complications were similar (10.9% vs. 14.0%, P = 0.590). In addition, the median overall survival was comparable between the two groups (20.0 vs. 18.7 months, P = 0.293).

Conclusion

LPD was found to be technically feasible with efficacy similar to OPD for patients with PDAC.

Application of erector spinae plane block guided by ultrasound for postoperative analgesia in breast cancer surgery: A randomized controlled trial
Tập 40 Số 2-3 - Trang 122-125 - 2020
Wensheng He, Zhenyu Wu, Lingjie Zu, Hai-Jun Sun, Xiaochun Yang
Associations of PGK1 promoter hypomethylation and PGK1‐mediated PDHK1 phosphorylation with cancer stage and prognosis: a TCGA pan‐cancer analysis
- 2019
Fei Shao, Xueying Yang, Wei Wang, Juhong Wang, Wei Guo, Xiaoli Feng, Susheng Shi, Qi Xue, Shugeng Gao, Yibo Gao, Zhimin Lu, Jie He
AbstractBackground

Cancer cells reprogram metabolism for proliferation. Phosphoglycerate kinase 1 (PGK1), as a glycolytic enzyme and newly identified protein kinase, coordinates glycolysis and mitochondrial metabolism. However, the clinical significance of PGK1 expression and function in cancer progression is unclear. Here, we investigated the relationship between the progression and prognosis of multiple cancer types and PGK1 expression and its function in the mitochondrial metabolism regulation.

Methods

We performed pan‐cancer analyses of PGK1 mRNA level and DNA methylation in 11,908 tumor tissues and 1582 paired normal tissues across 34 cancer types in The Cancer Genome Atlas datasets. Using specific antibodies against PGK1 S203 and PDHK1 T338 phosphorylation, we performed immunohistochemistry with tissue microarray assay in additional 818 cancer cases with 619 paired normal tissues from five cancer types.

Results

The PGK1 mRNA level was significantly elevated with hypomethylation in promotor regions and associated with advanced TNM stage in 15 and four cancer types, respectively. In breast carcinoma, elevated PGK1 mRNA level and promoter hypomethylation were associated with poor prognosis. Positively correlated PGK1 S203 and PDHK1 T338 phosphorylation levels were significantly associated with short overall survival (OS) in cancers of the breast, liver, lung, stomach, and esophagus and with advanced TNM stage in breast and esophageal cancers. PGK1 pS203 and PDHK1 pT338 were also independent predictors of short OS in liver, lung, and stomach cancer.

Conclusions

The elevated expression, promoter hypomethylation, and phosphorylation of PGK1 and PDHK1 were related with disease progression and short OS in diverse types of cancer. PGK1 and PDHK1 phosphorylation may be potential prognostic biomarkers.

Modulating the function of ABCB1: in vitro and in vivo characterization of sitravatinib, a tyrosine kinase inhibitor
Tập 40 Số 7 - Trang 285-300 - 2020
Yuqi Yang, Ning Ji, Chao‐Yun Cai, Jing‐Quan Wang, Zi‐Ning Lei, Qiu‐Xu Teng, Zhuo‐Xun Wu, Qingbin Cui, Yihang Pan, Zhe‐Sheng Chen
AbstractBackground

Overexpression of ATP‐binding cassette (ABC) transporter is a major contributor to multidrug resistance (MDR), in which cancer cells acquire resistance to a wide spectrum of chemotherapeutic drugs. In this work, we evaluated the sensitizing effect of sitravatinib, a broad‐spectrum tyrosine kinase inhibitor (TKI), on ATP‐binding cassette subfamily B member 1 (ABCB1)‐ and ATP‐binding cassette subfamily C member 10 (ABCC10)‐mediated MDR.

Methods

MTT assay was conducted to examine cytotoxicity and evaluate the sensitizing effect of sitravatinib at non‐toxic concentrations. Tritium‐labeled paclitaxel transportation, Western blotting, immunofluorescence analysis, and ATPase assay were carried out to elucidate the mechanism of sitravatinib‐induced chemosensitization. The in vitro findings were translated into preclinical evaluation with the establishment of xenograft models.

Results

Sitravatinib considerably reversed MDR mediated by ABCB1 and partially antagonized ABCC10‐mediated MDR. Our in silico docking simulation analysis indicated that sitravatinib strongly and stably bound to the transmembrane domain of ABCB1 human‐mouse chimeric model. Furthermore, sitravatinib inhibited hydrolysis of ATP and synchronously decreased the efflux function of ABCB1. Thus, sitravatinib could considerably enhance the intracellular concentration of anticancer drugs. Interestingly, no significant alterations of both expression level and localization of ABCB1 were observed. More importantly, sitravatinib could remarkably restore the antitumor activity of vincristine in ABCB1‐mediated xenograft model without observable toxic effect.

Conclusions

The findings in this study suggest that the combination of sitrvatinib and substrate antineoplastic drugs of ABCB1 could attenuate the MDR mediated by the overexpression of ABCB1.