This article summarizes Professor SHAN Zhaowei's clinical experience in treating chronic atrophic gastritis based on the "three-unblocking method". It is believed that spleen and stomach qi deficiency， qi stagnation and blood stasis is the core pathogenesis of chronic atrophic gastritis， with the key lying in the dysfunction of spleen and stomach transportation and descending. Therefore， the "three-unblocking method" was proposed， namely promoting the flow of yang and and removing turbidity to restore spleen transportation， unblocking the bowels to resolve stagnation and benefit qi movement， unblocking the meridians to resolve stasis and eliminate masses. In clinic， it is often combined with microscopic syndrome differentiation via gastroscopy. For those with spleen deficiency and damp obstruction， or yang qi failing to transport， the treatment should unblock yang to transform turbidity； for those with food retention and bowel obstruction， or stagnant qi movement， the treatment should unblock bowels to resolve stagnation； for those with blood stasis and meridian obstruction， or internal masses retention， the treatment should unblock the collaterals and dissolve stasis. The prescription can choose self-formulated Ershen Sancao Decoction （二参三草汤） and combine modification， showing good clinical effectiveness.

Recent studies have indicated that the expression of ubiquitin-specific protease 51 (USP51), a novel deubiquitinating enzyme (DUB) that mediates protein degradation as part of the ubiquitin‒proteasome system (UPS), is associated with tumor progression and therapeutic resistance in multiple malignancies. However, the underlying mechanisms and signaling networks involved in USP51-mediated regulation of malignant phenotypes remain largely unknown. The present study provides evidence of USP51's functions as the prominent DUB in chemoresistant triple-negative breast cancer (TNBC) cells. At the molecular level, ectopic expression of USP51 stabilized the 78 kDa Glucose-Regulated Protein (GRP78) protein through deubiquitination, thereby increasing its expression and localization on the cell surface. Furthermore, the upregulation of cell surface GRP78 increased the activity of ATP binding cassette subfamily B member 1 (ABCB1), the main efflux pump of doxorubicin (DOX), ultimately decreasing its accumulation in TNBC cells and promoting the development of drug resistance both in vitro and in vivo. Clinically, we found significant correlations among USP51, GRP78, and ABCB1 expression in TNBC patients with chemoresistance. Elevated USP51, GRP78, and ABCB1 levels were also strongly associated with a poor patient prognosis. Importantly, we revealed an alternative intervention for specific pharmacological targeting of USP51 for TNBC cell chemosensitization. In conclusion, these findings collectively indicate that the USP51/GRP78/ABCB1 network is a key contributor to the malignant progression and chemotherapeutic resistance of TNBC cells, underscoring the pivotal role of USP51 as a novel therapeutic target for cancer management.

Objective:To investigate the effect of Ureaplasma spp.lipid-associated membrane proteins(LAMPs)on macro-phage M1 polarization,and clarify how LAMPs resist to ferroptosis by regulating macrophage M1 polarization.The overall goal is to contribute to a better understanding of pathogenesis of non-gonococcal urethritis caused by Ureaplasma spp.Methods:ELISA,qPCR and flow cytometry were used to analyze the effect of LAMPs on M1 polarization of macrophages;Western blot to detect how LAMPs stimulates NF-κB pathway during M1 polarization of macrophages;gene interference technology was used to elucidate how LAMPs affects macrophage M1 polarization through regulating NF-κB pathway;CCK8 and Western blot were used to find out how LAMPs affects macrophage ferroptosis by regulating NF-κB pathway.Results:ELISA,qPCR and flow cytometry results showed that LAMPs promoted macrophage polarization to M1;Western blot results showed that LAMPs increased levels of p-p65 in macrophages;interfering with p65 expression could inhibit M1 polarization process of macrophages that mediated by LAMPs,and inhibition of macrophage ferroptosis that mediated by LAMPs could be significantly reversed.Conclusion:LAMPs inhibits ferroptosis by accelerating macrophage M1 po-larization,which is one of the important pathogenic factors of non-gonococcal urethritis caused by Ureaplasma spp.

Objective:To investigate factors influencing 18F-FDG PET/CT SUVmax,T/MB ratio and Ki-67 expression in non-Hodgkin's lymphoma(NHL),to analyze their correlations with lymphoma aggressiveness and their potential advantages in predicting therapeutic efficacy.Methods:A retrospective analysis was conducted to investigate correlations between tumor SUVmax,T/MB ratio,and Ki-67 expression with NHL aggressiveness and clinical characteristics in 99 patients;whether SUVmax,T/MB ratio and Ki-67 served as independent prognostic factors influencing therapeutic efficacy was examined,and potential utility of ΔSUVmax and ΔT/MB as biomarkers for treatment response assessment were evaluated.Results:Aggressive NHL demonstrated significantly higher SUVmax,T/MB ratio and Ki-67 level compared to indolent NHL and aggressive/indolent NHL(P<0.05).A pretreatment SUVmax≥9.05,T/MB≥5.115 or Ki-67≥55%could predict clinical remission in NHL patients post-treatment,while post-treatment reductions of ΔSUVmax≥22.65%or ΔT/MB≥34.85%were associated with achieved clinical remission.Conclusion:SUVmax,T/MB ratio and Ki-67 are closely associated with aggressiveness of NHL,which can be predicted whether NHL will be relieved after treatment.ΔSUVmax and ΔT/MB can assess whether NHL has been relieved after treatment.

Objective:To investigate the effect of Ureaplasma spp.lipid-associated membrane proteins(LAMPs)on macro-phage M1 polarization,and clarify how LAMPs resist to ferroptosis by regulating macrophage M1 polarization.The overall goal is to contribute to a better understanding of pathogenesis of non-gonococcal urethritis caused by Ureaplasma spp.Methods:ELISA,qPCR and flow cytometry were used to analyze the effect of LAMPs on M1 polarization of macrophages;Western blot to detect how LAMPs stimulates NF-κB pathway during M1 polarization of macrophages;gene interference technology was used to elucidate how LAMPs affects macrophage M1 polarization through regulating NF-κB pathway;CCK8 and Western blot were used to find out how LAMPs affects macrophage ferroptosis by regulating NF-κB pathway.Results:ELISA,qPCR and flow cytometry results showed that LAMPs promoted macrophage polarization to M1;Western blot results showed that LAMPs increased levels of p-p65 in macrophages;interfering with p65 expression could inhibit M1 polarization process of macrophages that mediated by LAMPs,and inhibition of macrophage ferroptosis that mediated by LAMPs could be significantly reversed.Conclusion:LAMPs inhibits ferroptosis by accelerating macrophage M1 po-larization,which is one of the important pathogenic factors of non-gonococcal urethritis caused by Ureaplasma spp.

Objective:To investigate factors influencing 18F-FDG PET/CT SUVmax,T/MB ratio and Ki-67 expression in non-Hodgkin's lymphoma(NHL),to analyze their correlations with lymphoma aggressiveness and their potential advantages in predicting therapeutic efficacy.Methods:A retrospective analysis was conducted to investigate correlations between tumor SUVmax,T/MB ratio,and Ki-67 expression with NHL aggressiveness and clinical characteristics in 99 patients;whether SUVmax,T/MB ratio and Ki-67 served as independent prognostic factors influencing therapeutic efficacy was examined,and potential utility of ΔSUVmax and ΔT/MB as biomarkers for treatment response assessment were evaluated.Results:Aggressive NHL demonstrated significantly higher SUVmax,T/MB ratio and Ki-67 level compared to indolent NHL and aggressive/indolent NHL(P<0.05).A pretreatment SUVmax≥9.05,T/MB≥5.115 or Ki-67≥55%could predict clinical remission in NHL patients post-treatment,while post-treatment reductions of ΔSUVmax≥22.65%or ΔT/MB≥34.85%were associated with achieved clinical remission.Conclusion:SUVmax,T/MB ratio and Ki-67 are closely associated with aggressiveness of NHL,which can be predicted whether NHL will be relieved after treatment.ΔSUVmax and ΔT/MB can assess whether NHL has been relieved after treatment.

Objective To analyze the medication laws of children with nephrotic syndrome during hormone withdrawal period treated by TCM master Zhang Qi using data mining methods,inheriting his academic ideas.Methods The medical records of children with nephrotic syndrome during the hormone withdrawal period treated by Professor Zhang Qi at the Outpatient Department of Traditional Chinese Medicine of Heilongjiang Provincial Hospital from January 2008 to December 2018 were collected.A database was established using Excel 2019.Frequency statistics,association rules,and clustering analysis were employed among other data mining techniques to elucidate Professor Zhang Qi's medication principles based on the Traditional Chinese Medicine Inheritance Computing Platform 3.5.Results A total of 271 prescriptions were selected,encompassing 194 types of Chinese herbs,with a total drug frequency of 4 610 instances.High-frequency herbs included Glycyrrhizae Radix et Rhizoma,Astragali Radix,Nelumbinis Semen,Ophiopogonis Radix,Lycii Cortex,Poria,Pseudostellariae Radix,Bupleuri Radix,Lonicerae Japonicae Flos,and others.The properties of the drugs were predominantly cold and neutral,with flavors mainly sweet,bitter and pungent,and they targeted the lung meridian,spleen meridian,and kidney meridian primarily.In terms of therapeutic efficacy,there was a higher frequency of usage for tonifying deficiencies,clearing heat,and resolving water and dampness.Through association rule analysis,a total of 184 groups of high-frequency herb combinations were identified.When the support rate was set at 60%,seven core herb combinations were included:Astragali Radix,Pseudostellariae Radix,Nelumbinis Semen,Ophiopogonis Radix,Lycii Cortex,Poria,Glycyrrhizae Radix et Rhizoma.Clustering analysis yielded 6 novel formula combinations.Conclusion The hormone withdrawal period for children with nephrotic syndrome is characterized by the weakness of the lung,spleen and kidney,commonly presenting as qi-yin deficiency syndrome.Professor Zhang Qi manages the condition by regulating the qi of the lung,spleen and kidney,and employs a treatment strategy that is both tonifying and supplementing.To balance yin and yang,medications are chosen to clear dampness and heat,regulate qi and the stomach,and promote the elimination of water and dampness.

Aim To construct a diabetic atherosclerosis mouse model and study the pathological characteristics of diabetic atherosclerosis.Methods Fifty 8-week-old male LDLR-/-mice were fed with standard diet for 2 weeks and then changed to high-fat diet,they were randomly divided into two groups.The diabetic atherosclerosis group was given intraperitoneal injection of low dose streptozotocin(STZ)for 5 days continuouly to establish the model,and the atheroscle-rosis group was given citrate buffer injection at the same time.The body mass,blood glucose and blood lipids of the mice in the two groups were detected for many times.At the age of 23 weeks,the mice were euthanized after glucose tolerance test.HE staining and oil red O staining were used to detect the gross and aortic root atherosclerosis,immunohistochemical staining was used to detect CD4,α-smooth muscle actin(α-SMA),EGF-like module-containing mucin-like hormone re-ceptor-like 1(EMR1),monocyte chemotactic protein-1(MCP-1),NOD-like receptor protein 3(NLRP3),vascular cell adhesion molecule-1(VCAM-1),matrix metalloproteinase-2(MMP-2)and tissue inhibitor of metalloproteinase-1(TIMP-1),Western blot was used to detect α-SMA,CD4,tumor necrosis factor-α(TNF-α),NLPR3,intercellular adhesion molecule-1(ICAM-1),and type Ⅰ and Ⅲ collagen.Results Compared with the atherosclerosis group,the body mass decreased,the levels of total cholesterol(TC),triglyceride(TG),low density lipoprotein cholesterol(LDLC)increased,and the levels of high density lipoprotein cholesterol(HDLC)decreased(P＜0.05)in the diabetic atherosclerosis group.Compared with the atherosclerosis group,the distribution of atherosclerotic plaques was diffuse and the area was increased in the diabetic atherosclerosis group,and the contents of lipids,T cells,macrophages,smooth muscle cells,type Ⅰ and Ⅲ colla-gen were increased(P＜0.05);the protein levels of TNF-α,MCP-1,MMP-2,NLRP3,ICAM-1 and VCAM-1 in vascular tissues were increased,while the content of TIMP-1 were decreased and MMP2/TIMP-1 were increased(P＜0.05).Conclusions LDLR-mouse model of diabetic atherosclerosis can be successfully established by STZ induction combined with high-fat diet,which can reflect the plaque composition and inflammatory characteristics of diabetes promoting atheroscle-rosis.It can be used as a relatively ideal pathological model for the study of diabetic macroangiopathy.

Background::Breast cancer is ranked among the most prevalent malignancies in the Chinese female population. However, comprehensive reports detailing the latest epidemiological data and attributable disease burden have not been extensively documented.Methods::In 2018, high-quality cancer surveillance data were recorded in 700 population-based cancer registries in China. We extracted data on female breast cancers (International Classification of Diseases, Tenth Revision [ICD-10]: C50) and estimated the incidence and mortality in 2022 according to the baseline data and corresponding trends from 2010 to 2018. Pathological types were classified according to the ICD for Oncology, 3rd Edition codes. Disability-adjusted life years (DALYs) were calculated as the sum of the years of life lost (YLLs) and years lived with disability (YLDs).Results::In 2022, approximately 357,200 new female breast cancer cases and 75,000 deaths occurred in China, accounting for 15.59% and 7.94% of total new cancer cases and deaths, respectively. The age-standardized incidence rate (ASIR) was 33.04 per 100,000. When analyzed by pathological type, the ASIRs for papillary neoplasms, invasive breast carcinoma, rare and salivary gland-type tumors, and other types were 1.13, 29.79, 0.24, and 1.88 per 100,000, respectively. The age-standardized mortality rate (ASMR) was 6.10 per 100,000. A total of 2,628,000 DALYs were found to be attributable to female breast cancer in China, comprising 2,278,300 YLLs and 349,700 YLDs. The ASIR, ASMR, and age-standardized rate (ASR) for DALYs in urban areas were consistently higher than those in rural areas. We observed a four-fold increase in the ASIR and ASR for DALYs and an eight-fold increase in the ASMR among females over 55 years compared with those aged under 55 years.Conclusion::These data provide invaluable insights into the latest epidemiology of female breast cancer in China and highlight the urgency for disease prevention and control strategy formulation.

Bioactive compounds derived from herbal medicinal plants modulate various therapeutic targets and signaling pathways associated with cardiovascular diseases (CVDs), the world's primary cause of death. Ginkgo biloba, a well-known traditional Chinese medicine with notable cardiovascular actions, has been used as a cardio- and cerebrovascular therapeutic drug and nutraceutical in Asian countries for centuries. Preclinical studies have shown that ginkgolide B, a bioactive component in Ginkgo biloba, can ameliorate atherosclerosis in cultured vascular cells and disease models. Of clinical relevance, several clinical trials are ongoing or being completed to examine the efficacy and safety of ginkgolide B-related drug preparations in the prevention of cerebrovascular diseases, such as ischemia stroke. Here, we present a comprehensive review of the pharmacological activities, pharmacokinetic characteristics, and mechanisms of action of ginkgolide B in atherosclerosis prevention and therapy. We highlight new molecular targets of ginkgolide B, including nicotinamide adenine dinucleotide phosphate oxidases (NADPH oxidase), lectin-like oxidized LDL receptor-1 (LOX-1), sirtuin 1 (SIRT1), platelet-activating factor (PAF), proprotein convertase subtilisin/kexin type 9 (PCSK9) and others. Finally, we provide an overview and discussion of the therapeutic potential of ginkgolide B and highlight the future perspective of developing ginkgolide B as an effective therapeutic agent for treating atherosclerosis.