Chao Ni
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View article: PersADE: a database of personalized adverse drug events and their underlying molecular mechanisms
PersADE: a database of personalized adverse drug events and their underlying molecular mechanisms Open
As a major burden on global healthcare systems, adverse drug events (ADEs) result in significant morbidity, mortality, and healthcare resource consumption. With the rapid advances in precision medicine, personalized ADEs and their molecula…
View article: Dietary index for gut microbiota, genetic risk, and incidence of breast cancer: a prospective study
Dietary index for gut microbiota, genetic risk, and incidence of breast cancer: a prospective study Open
View article: Cancer cells impede T cell early activation and drive immune evasion by transferring Tmem176b
Cancer cells impede T cell early activation and drive immune evasion by transferring Tmem176b Open
Despite its remarkable clinical success in human cancer treatment, immune checkpoint blockade is effective only in a minority of patients. One major obstacle is tumor-driven impairment of T cell priming and early activation, however, the u…
View article: Tumor battlefield within inflamed, excluded or desert immune phenotypes: the mechanisms and strategies
Tumor battlefield within inflamed, excluded or desert immune phenotypes: the mechanisms and strategies Open
The tumor microenvironment demonstrates great immunophenotypic heterogeneity, which has been leveraged in traditional immune-hot/cold tumor categorization based on the abundance of intra-tumoral immune cells. By incorporating the spatial i…
View article: Immune mediated support of metastasis: Implication for bone invasion
Immune mediated support of metastasis: Implication for bone invasion Open
Bone is a common organ affected by metastasis in various advanced cancers, including lung, breast, prostate, colorectal, and melanoma. Once a patient is diagnosed with bone metastasis, the patient's quality of life and overall survival are…
View article: FOXA3 regulates cholesterol metabolism to compensate for low uptake during the progression of lung adenocarcinoma
FOXA3 regulates cholesterol metabolism to compensate for low uptake during the progression of lung adenocarcinoma Open
Cholesterol metabolism is vital for multiple cancer progression, while how cholesterol affects lung, a low-cholesterol tissue, for cancer metastasis and the underlying mechanism remain unclear. In this study, we found that metastatic lung …
View article: Supplementary Figure S7 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S7 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S7. CD24hiCD27+ Bregs induce drug resistance by activating NF-kB and STAT3 signalling in BC cells with effect stronger when in a direct contact.
View article: Supplementary Figure S2 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S2 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S2. Comparison of CD24hiCD27+ Bregs from peripheral blood and LNs.
View article: Supplementary Figure S9 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S9 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S9. CD24hiCD27+ Bregs are the main cellular sources of IL-10, IL-6 and TNF-α among CD45+ immune cells within the mLNs.
View article: Supplementary Figure S1 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S1 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S1. The features of B cells in the mLNs of BC.
View article: Supplementary Figure S4 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S4 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S4. CD24hiCD27+ Breg-induced drug resistance in BC is independent of small molecule substances.
View article: Supplementary Table S4 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Table S4 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Table. S4. Characteristics of the patient samples and basic information.
View article: Supplementary Figure S10 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S10 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S10. CD24hiCD27+ Bregs induce the upregulation of CD40L and PD-L1 in BC cells.
View article: Supplementary Figure S1 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S1 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S1. The features of B cells in the mLNs of BC.
View article: Supplementary Figure S12 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S12 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S12. The addition of anti-PD1/PD-L1 to neoadjuvant chemotherapy improves the pCR rate of patients with mLNs.
View article: Supplementary Figure S8 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S8 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S8. Depletion of B cells within the LNs of mice by anti-CD20 antibody injection.
View article: Supplementary Figure S11 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S11 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S11. Anti-PD-L1 treatment attenuates the activation of B cells and improves the treatment response rate of mLNs.
View article: Supplementary Table S2 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Table S2 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Table. S2. Annotation of the 92 Olink biomarkers studied herein.
View article: Supplementary Figure S5 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S5 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S5. Direct cell-cell contact between BC cells and CD24hiCD27+ Bregs endows BC cells with stronger stemness and drug resistance.
View article: Supplementary Table S1 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Table S1 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Table. S1. List of antibodies used in this study.
View article: Supplementary Figure S6 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S6 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S6. CD24hiCD27+ Bregs induce the drug resistance of BC cells by secreting IL-6 and TNF-α.
View article: Supplementary Table S1 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Table S1 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Table. S1. List of antibodies used in this study.
View article: Supplementary Figure S3 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S3 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S3. CD24hiCD27+ Bregs induce epithelial-mesenchymal transition and stemness of BC cells.
View article: Supplementary Figure S6 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S6 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S6. CD24hiCD27+ Bregs induce the drug resistance of BC cells by secreting IL-6 and TNF-α.
View article: Supplementary Figure S12 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S12 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S12. The addition of anti-PD1/PD-L1 to neoadjuvant chemotherapy improves the pCR rate of patients with mLNs.
View article: Supplementary Figure S10 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S10 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S10. CD24hiCD27+ Bregs induce the upregulation of CD40L and PD-L1 in BC cells.
View article: Supplementary Figure S9 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S9 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S9. CD24hiCD27+ Bregs are the main cellular sources of IL-10, IL-6 and TNF-α among CD45+ immune cells within the mLNs.
View article: Supplementary Figure S3 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S3 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S3. CD24hiCD27+ Bregs induce epithelial-mesenchymal transition and stemness of BC cells.
View article: Supplementary Table S4 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Table S4 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Table. S4. Characteristics of the patient samples and basic information.
View article: Supplementary Figure S5 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer
Supplementary Figure S5 from CD24<sup>hi</sup>CD27<sup>+</sup> Bregs within Metastatic Lymph Nodes Promote Multidrug Resistance in Breast Cancer Open
Fig. S5. Direct cell-cell contact between BC cells and CD24hiCD27+ Bregs endows BC cells with stronger stemness and drug resistance.