key: cord-0699614-9wvc6zae
authors: Dong, Qiang; Li, Qiao; Duan, Lei; Wang, Hongyu; Yan, Yunji; Yin, Hang; Niu, Liang; Zhang, He; wang, Bo; Yuan, Guoqiang; Pan, Yawen
title: Expressions and significances of CTSL, the target of COVID‐19 on GBM
date: 2021-11-22
journal: J Cancer Res Clin Oncol
DOI: 10.1007/s00432-021-03843-9
sha: c6a129f943ce9811f8a5d30d30354e757426918d
doc_id: 699614
cord_uid: 9wvc6zae

INTRODUCTION: Cathepsin L (CTSL) is a kind of the SARS-entry-associated CoV-2's proteases, which plays a key role in the virus's entry into the cell and subsequent infection. We investigated the association between the expression level of CTSL and overall survival in Glioblastoma multiforme (GBM) patients, to better understand the possible route and risks of new coronavirus infection for patients with GBM. METHODS: The expression level of CTSL in GBM was analyzed using TCGA and CGGA databases. The relationship between CTSL and immune infiltration levels was analyzed by means of the TIMER database. The impact of CTSL inhibitors on GBM biological activity was tested. RESULTS: The findings revealed that GBM tissues had higher CTSL expression levels than that of normal brain tissues, which was associated with a significantly lower survival rate in GBM patients. Meanwhile, the expression level of CTSL negatively correlated with purity, B cell and CD8(+) T cell in GBM. CTSL inhibitor significantly reduced growth and induced mitochondrial apoptosis. CONCLUSION: According to the findings, CTSL acts as an independent prognostic factor and can be considered as promising therapeutic target for GBM. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00432-021-03843-9.

Coronavirus disease 2019 (COVID-19) is highly infectious and transmitted mainly by inhaling droplets or aerosols released by an infected individual and possibly by a feco-oral transmission route, has accumulated 160,317,950 confirmed cases globally until mid-May 2021 (https:// www. world omete rs. info/ coron avirus/). Understanding the mechanism of action of the virus is an important step in determining the best treatment. It has been reported that SARS-CoV2 enters host cells via spike proteins that bind to the angiotensinconverting enzyme 2 (ACE2) membrane-bound protein (Gemmati et al. 2020) . After binding to target cells, the S protein is cleaved into two subunits: S1 and S2 by TMPRSS2 and host cell proteases such as cathepsin L (CTSL), which promotes viral entry into the cell by inducing membrane fusion and endocytosis of several coronaviruses. This cleavage of S protein by host proteases is critical for viral activation and subsequent infection Hoffmann et al. 2020) . Infection by SARS-CoV-2 results in significant morbidity and mortality. While the lung is the major organ of infection, some studies implied that SARS-CoV-2 might invade the CNS, causing neurological disorders (Narayanappa et al. 2021) . Neurological symptoms, such as headache, dizziness, and impaired consciousness as well as symptoms involving the cranial nerves have been reported in COVID-19 patients (Achar and Ghosh 2020) .

CTSL, a member of the lysosomal cysteine protease family, plays a role in lysosomal protein degradation in most cell types (Nakagawa 1998) . CTSL expressing on the surface of cancer cells and secreted into the extracellular matrix to Qiang Dong and Qiao Li contributed equally to this work. degrade extracellular matrix components. CTSL preferentially cleaves the peptide bond between the aromatic residue at the p2 position and the hydrophobic residue at the P3 position (Brady et al. 2000) . The acidic environment in lysosomes promotes the activation of proteolytic enzymes. In addition, the locally acidic environment caused by anaerobic glycolysis also activates extracellular CTSL, which encourages the invasion of cancer cells into surrounding tissues, blood and lymphatic vessels, and the metastasis of tumor tissue to distant tissues (Sudhan and Siemann 2013) . Previous studies have shown that the high expression of CTSL significantly promotes the proliferation, invasion, migration, drug resistance and angiogenesis in lung cancer, gastric cancer, ovarian cancer, breast cancer, glioma and other malignant tumors (Yao et al. 2018; Sigloch et al. 2017) . Shan et al. (2016) found that the over-expressed transcription factor Forkhead box O3a (FOXO3a) in gastric cancer cells can activate the promoter of CTSL, inhibit the expression of E-cadherin, and promote the development of gastric cancer. CTSL inhibitors can reduce the tumor model's ability to form blood vessels (Sudhan et al. 2016) .

The pathogenesis of tumors is relatively complex, involves a variety of pathophysiological processes, and is affected by a variety of factors, among which the immune status of the body cannot be ignored. In the process of tumor occurrence and development, the immune response of the organism is often weakened (Leskowitz et al. 2015) . Due to the low immune function of patients with malignant tumors and the suppression of the systemic immune system caused by anti-tumor treatments such as radiotherapy and chemotherapy or surgery, tumor patients are more susceptible to SARS-CoV2 than non-tumor patients (Addeo and Friedlaender 2020) . In addition, the expression of SARS-CoV2 receptors (ACE2, CTSL and TMPRSS2) significantly increased in many kinds of tumors, which makes viral entry into the cell and cancer patients more susceptible to SARS-CoV2 (Bao et al. 2020) .

Analyses of the expression and related biological processes of CTSL in GBM are useful to aid in the understanding of COVID-19 pathogenesis and the development of therapeutic strategies. In the present study, CTSL expression was identified using TCGA and GEPIA databases. Furthermore, the diagnostic and prognostic values of CTSL in GBM were determined. Subsequently, we evaluated whether CTSL can be regarded as a therapeutic target for GBM.

CTSL inhibitor 1 was purchased from Selleck Chemicals (Shanghai, China). Cell Counting Kit-8 (CCK-8) was purchased from Dojindo Molecular Technologies (Kumamoto, Japan). PE Annexin V apoptosis detection commercial kit were purchased from BD Biosciences (Shanghai, China). Cell-Light EdU Apollo567 in Vitro Kit was purchased from Guangzhou Ruibo Biotechnology Co. LTD (Guangzhou, China). Anti-CTSL, anti-Bax, anti-Bcl-2 and anti-MMP-9 antibodies were obtained from Proteintech (Wuhan, China). Anti-GAPDH was purchased from Abcam (Cambridge, UK).

The Cancer Genome Atlas (TCGA; https:// www. cancer. gov/ tcga) was used to obtain GBM RNA-seq data. A total of 35 GBM and 16 normal brain tissue samples were acquired with signed informed consent from Lanzhou University Second Hospital. Normal brain tissue samples were obtained from patients without glioma who underwent surgery for other reasons, including cerebral trauma. All procedures involving human samples were approved by the Ethics Committee of Lanzhou University Second Hospital.

The prognostic value of CTSL was analyzed using CGGA (http:// www. cgga. org. cn/). The overall survival (OS) rates of the patients in the high-level and low-level GBM groups were evaluated using Kaplan-Meier analysis.

TIMER is a database (https:// cistr ome. shiny apps. io/ timer/) for systematic analysis of immune information of various types of tumors (Deng et al. 2020) . The TIMER database contains data from a total of 10,897 samples of 32 cancers from TCGA and can assess the abundance of tumor immune infiltration. The "Gene" module was used to analyze the correlation between the expression level of CTSL and the abundance of immune cell infiltration in GBM.

Total RNA was extracted from tissues using TRIzol reagent (Invitrogen). Then, reverser anscribed with the reverse transcription kit (RR037A, Takara Bio, Japan). The expression of mRNAs of CTSL were determined with a LightCycler (RR390Q, Takara Bio, Japan) using TB SYBR green Premix Ex Taq II (Takara Bio, Japan). And the results were analyzed by 2 −ΔΔCT method. The following primers were used: CTSL forward, 5'-GAA AGG CTA CGT GAC TCC TGTG -3' and reverse, 5'-CCA GAT TCT GCT CAC TCA GTGAG -3'; GAPDH, forward 5'-GGA CCT GAC CTG CCG TCT AG -3' and reverse, 5'-TAG CCC AGG AGG ATG CCC TTG AG-3'.

U251 cells were inoculated in 96-well plates and treated with BCA for 24 h, 48 h and 72 h. Each well is added 10 µL of CCK8, incubated for 2 h at 37 °C incubator, and then detected absorbance with a microplate reader. U251 cells were seeded in 96-well plates, each well is added 100 µL of 50 uM Edu solution, incubated for 2 h at 37 °C incubator, and then 4% Paraformaldehyde fixation. Wash with PBS for three times, and each well is added 100 µL 1 × Hoechst33342 solution, incubated at 37 °C in the dark for 30 min, then observed and analyzed under a fluorescence microscope.

U251 cells were treated with 0, 50, and 100 μmol/L BCA for 48 h. Then, U251 cells (1 × 10 6 ) were collected, after which 5 µL of PE Annexin V and 5 µL of 7-AAD were added. Gently vortex the cells and incubate at 25 °C in the dark for 15 min and the suspension was analyzed by flow cytometry (BD FACSCanto™ low cytometry, USA).

CTSL inhibitor-treated U251 cells were inoculated into a six-well plate. When the cells reach a confluence of 70-80%, were gently and slowly scratched with a new 200 µL pipette tip. The relative distance of the cells migrating was monitored and measure using a bright-field microscope at 0, 12 and 24 h.

Transwell chambers membrane was pre-coated with diluted Matrigel (1:8 BD Biosciences). About 1 × 10 6 cells in 100 µL serum-free medium were added into the top chambers, and 600 µL DMEM medium was added into the lower chamber. After 24 h. the chambers were washed and cells were fixed in 4% paraformaldehyde, and subsequently stained with 0.1% crystal violet. Cell invasion assay was performed as above except used the cell culture inserts coated with Matrigel (BD Biosciences).

U251 cells (2 × 10 6 ) were lysed using RIPA buffer (Solarbio, China). The lysed cells were centrifuged at 12,000×g for 10 min at 4 °C. Proteins were loaded on 10% SDS-PAGE gels and transferred onto PVDF membranes. The band was visualized by enhanced chemiluminescence with image-Quant LAS 500 system.

SPSS version 23.0 (IBM, Armonk, NY, USA), GraphPad Prism 8.0 (GraphPad, San Diego, CA, USA) and R software v4.0.3 (R Foundation for Statistical Computing, Vienna, Austria) were used to perform statistical analyses and graphing. Survival curves were estimated using the Kaplan-Meier method with the log-rank test. P < 0.05 was considered significant.

To elucidate the expression of CTSL in GBM, we analyzed the TCGA and GEPIA database. The level of CTSL expression was markedly upregulated in GBM (P < 0.05; Fig. 1A , B). The expression level of CTSL was confirmed using RT-qPCR and western blotting in GBM tissues (n = 35) and normal brain tissues (n = 16) to confirm the GEPIA database findings. The results showed that the level of CTSL was significantly increase in GBM (P < 0.05; Fig. 1C , D). Meanwhile, the data was consistent with TCGA and GEPIA database analysis. The correlation between the clinicopathological characteristic and the expression of CTSL was evaluated in the cases of 35 GBM patients. The median mRNA level of CTSL was used as a cut-off value. However, the CTSL expression levels was not significantly associated with any of the other parameters assessed, including age, sex, and Karnofsky Performance Status (P > 0.05) ( Table 1 ).

To determine whether CTSL can been regarded as an independent prognostic factor for GBM patients, the correlation between OS and the expressions of CTSL was evaluated in the cases of GBM patients using Kaplan-Meier analysis and log-rank tests. The results indicated that patients with high expression of CTSL had a lower OS rate than patients with low expression of CTSL (P = 0.035; Fig. 2D ). In addition, we further verified the results coming from TCGA and CGGA databases (Fig. 2B, C) . To further identify the diagnostic value of CTSL in GBM patients, ROC curve analysis was performed. The results showed (Fig. 2E) (Fig. 2E) . It is suggested that the CTSL has higher prognostic value in the GBM. Furthermore, the correlations between CTSL expression and major clinic pathological factors were determined using Cox regression analysis. Univariate Cox regression analysis revealed that CTSL expression was an independent prognostic factor for OS in patients with GBM (hazard ratio, 3.599; 95% CI 1.260-10.278; P = 0.017; Fig. 2F ).

To have a better understanding of CTSL and the tumor immune microenvironment, we analysis the relationship between CTSL expression and tumor immune infiltration using TIMER database. Purity of the tumor means the tumor cell proportion in the tissue. The results showed that CTSL was very negatively correlated with purity (r = − 0.375, P < 0.001), B cell (r = − 0.138, P < 0.01) and CD8 + T cell (r = − 0.246, P < 0.001). However, the expression of CTSL was positively correlated with the level of immune infiltration of dendritic cell neutrophil (r = 0.211, P < 0.001) and dendritic cell (r = 0.63, P < 0.001) in GBM (Fig 3) .

To evaluate the cytotoxic effect of cathepsin inhibitor 1 to GBM, U251 cells were seed in 96-well plates and treated with different concentration of BCA for24, 48 and 72 h, and The CTSL mRNA expression level was analyzed in GEPIA database. C Expression of CTSL mRNA in GBM tissues were tested by RT-qPCR. D The protein expression levels of CTSL in patients with GBM were analyzed by western blotting. *P < 0.05 and ****P < 0.001 cell viability was measured using the CCK-8. As shown in Fig. 4A , cell viability decreased following treatment with cathepsin inhibitor 1 in a concentration-dependent manner. In addition, the Edu assay was performed to determine the effect of cathepsin inhibitor 1 on GBM cell proliferation. cathepsin inhibitor 1 treatment significantly increased the percentage of Edu-positive cells compared with the control (Fig. 4B) . Taken together, these data indicated that cathepsin inhibitor 1 inhibited the growth of U251 cells in a concentration-dependent manner. To evaluate the effects of cathepsin inhibitor 1 on GBM cells migration, we performed wound healing assay. For this experiment, U251 cells were cultured and then co-incubated with different doses (0, 50 and 100 μM) of CTSL-1for various time intervals (0, 12 and 24 h). Treatment with various doses of cathepsin inhibitor 1 for 12 and 24 h significantly decreased cell migration rates in U251 cells (Fig. 4C, D) . We also examined cell migration and invasion capacity using a transwell chambers system after the indicated cell lines were treated with different doses (0, 50 and 100 μM) of CTSL-1 (Fig. 4E , F, G). U251 cells significantly decreased migration and invasion rates significantly in a dose-dependent manner, which was consistent with the cell wound healing assay. These results showed that cathepsin inhibitor 1 inhibits U251 cell migration and invasion in vitro.

To verify whether CTSL-1 induced proliferation in an apoptosis-related manner, the effect of cathepsin inhibitor 1 on the apoptosis of U251 cells was examined using flow cytometry. We found that cathepsin inhibitor 1 treatment significantly increased the apoptosis of U251 cells (Fig. 5A,  B) . Meanwhile, we further detect molecular markers related to apoptosis. After treatment of cathepsin inhibitor 1, the expression of CTSL and anti-apoptosis protein BCL-2 expression markedly decrease, and pro-apoptosis protein Bax expression increase (Fig. 5C-G) . Thus, these findings show that cytotoxic effects of cathepsin inhibitor 1 on U251 cells were partly caused by activation mitochondria-mediated intrinsic apoptotic pathway.

In December 2019, a novel coronavirus (2019-nCov) has caused large-scale pandemics, which has caused a severe challenge for public health and the economy (Xie and Chen 2020) . A large number of studies have described the mechanism by which the SARS-CoV-2 virus enters the cell. Although, it has been widely reported that SARS-CoV2 promotes its entry into host cells through the spike protein that binds to the angiotensin-converting enzyme 2 (ACE-2) membrane-bound protein . CTSL seems to be responsible for the cleavage of S protein under different circumstances (Vargas-Alarcón et al. 2020) . Therefore, understanding the regulation of viral entry in a comorbid state will also require understanding the expression of these genes. In this study, we analysis the CTSL mRNA level of GBM in GEPIA and TCGA database. We evaluated the relationship between the expression of CTSL and the prognosis of GBM patients who susceptibility to COVID-19. In addition, TIMER database was also used to analyze the correlation between CTSL and immune infiltration in GBM. Moreover, we used CTSL inhibitor to observe the effect on the proliferation, invasion, and apoptosis of GBM cells.

Recently studies demonstrated that cancer patients are confirmed to have a higher incidence of COVID-19, more severe symptoms and has a poor prognosis (Jacobo et al. 2020) . SARS-CoV-2 can undergo endocytosis, endosomal maturation followed by cleavage with pH-dependent cysteine protease CTSL to promote SARS-CoV-2 entry in cells. Recently study demonstrated that the down-regulation expression CTSL may be a potential mechanism that might reduce the ability of the virus to enter host cell, and regulation lysosome PH that would further interfere with proteolytic Spike protein activation may offer protection from the virus to enter (Kwan et al. 2021) . So, CTSL plays a vital role in SARS-CoV-2 to enter cells. Here, our data demonstrated that CTSL upregulates in the GBM. In addition, SARS-CoV-2 might invade the CNS, causing neurological disorders. There is currently no effective targeted drug to treat COVID-19. Although several countries have made great progress in researching COVID-19 vaccines, the vaccines are only effective for some person. A large number of studies have shown that some small molecule drugs have a good effect on the treatment of COVID-19, for example, melatonin , hydroxychloroquine and chloroquine (Sanders et al. 2020) . The main mechanism of these small molecule drugs is to inhibit virus entry by targeting the endocytic pathway (Merad and Martin 2020) . Hydroxychloroquine and chloroquine increase the pH of the endosome, thereby inhibiting membrane fusion, which is a necessary mechanism for the virus to enter the cell (Savarino et al. 2006 ). In addition, the glycosylation of ACE2 and S protein can be inhibited to inhibit virus infection of cells.

Cancer is a disorder with immune dysfunction, and cancer patients are more susceptible to infections (Wang and Zhang ). Both humoral and cellular immunity are involved in the resistance to SARS-CoV-2 infection in the body. There is evidence that the abnormal regulation of immune response, especially T cells, may be highly related to the pathological process of COVID-19 (Qin et al. 2020) . At the same time, others have also proved that abnormal and excessive immune cells (such as monocytes and macrophages) play a role in immune damage in COVID-19 (Merad and Martin 2020) . We used the TIMER database to further explore its correlation with immune cell infiltration. The result showed that CTSL was very negatively correlated with purity, B cell and CD8 + T cell. However, the expression of CTSL was positively correlated with the level of immune infiltration of dendritic cell neutrophil and dendritic cell in GBM.

In addition, Kaplan-Meier curves and the log-rank test result showed that down regulation of CTSL had a favorable prognosis in GBM patients. Therefore, we evaluated the prognosis of GBM infected with SARS-CoV-2 according to the expression level of CTSL. Previous studies have found that CTSL highly expressed not only in gliomas but also in a variety of tumors, such as lung cancer, gastric cancer, ovarian cancer, breast cancer and other malignant tumors. So, cancer patients may be more susceptible to the SARS-CoV-2 infectious disease.

Previous studies have showed that CTSL expression is associated with the prognosis of tumor patients. For example, CTSL is over expression in nasopharyngeal carcinoma, breast cancer and pediatric acute myeloid leukemia, and is associated with poor disease-free survival (Yao et al. 2018; Sigloch et al. 2017) . In this study, Kaplan-Meier survival analysis showed that patients with high CTSL levels had shorter OS and worse prognosis. Interestingly, evidence indicates that CTSL expression may be linked to the grade and stages of endometrial cancer patients. In addition, CTSL ablation can block angiogenesis in breast cancer by affecting cell cycle-associated genes, including cyclin D1-D3, E2, A2, B2 and H (Wang et al. 2019) . Wang et al. (2016) demonstrated that Knockdown of Cathepsin L can inhibit GSC growth and increase tumor radio-sensitivity by decreasing CD133 expression and decrease DNA repair checkpoint proteins (ATM and DNA-PKcs). Qin et al. (2016) demonstrated that CTSL can promote proliferation of breast cancer and downregulation of CTSL significantly inhibited the proliferation of MCF-7 cells. Moreover, CTSL can inhibited A549 and MCF-7 cells migration by regulating PI3K-AKT and Wnt signaling pathways.

Importantly, evidence indicates that CTSL proteolytic activity is significantly higher in tumor tissue compared to normal tissue. In normal tissues, the extracellular matrix is protected by endogenous cathepsin inhibitors (such as cysteine and stefins) from undesirable proteolytic activity.

However, studies have shown that the expression of these CTSL inhibitors declines sharply in various tumors and CTSL proteolytic activity increase. Therefore, the use of some exogenous CTSL inhibitors can reduce the expression and proteolytic activity of CTSL. For example, CTSL inhibitor KGP94 have anti-angiogenic efficacy, and can inhibited angiogenesis of breast cancer (Sudhan et al. 2016) . Sudhan et al. (2016) found that KGP94 treatment significantly attenuation of tumor cell invasion and migration that it may have significant utility as an anti-metastatic agent. This study has found that CTSL inhibitor 1 significantly reduced the growth, invasion, and migration of U251 cells in vitro and triggered mitochondrial apoptosis. Taken together, these findings suggest CTSL as a promising therapeutic target for clinical therapy in GBM patients. Therefore, because CTSL plays an important role in the pathogenesis of COVID-19, the targeted inhibition of CTSL may be an effective treatment option for this infectious disease.

In conclusion, higher expression of CTSL was found in GBM tissues compared with that of normal brain tissues, which resulted in significantly a poor survival rate in GBM Fig. 4 Cathepsin inhibitor 1 inhibited the proliferation, migration, and invasion of U251 cells. A U251 cells were treated with various concentrations BCA for 24, 48 and 72 h. Cell proliferation was measured by CCK8 assay. B Cellular proliferation was measured via an Edu assay. C Wound healing assay shows the migrated cells at 0, 12 and 24 h after treatment with CTSL-1 (0, 50 and 100 μM). D Quantification of the wound healing rate in A after treatment with BCA. E After treatment, transwell assay showed that the migration and invasion cells at 24 h. F, G Quantification of the migration and invasion cells. *P < 0.05 and **P < 0.01 for Student's t test patients. We considered the possible role of CTSL in the pathogenesis of COVID-19. Therefore, assessment of CTSL gene expression can be used to predict the prognosis and susceptibility to COVID-19 in these patient groups. CTSL inhibitors may be considered as promising treatments for GBM patients with SARS-CoV-2 infection.

The online version contains supplementary material available at https:// doi. org/ 10. 1007/ s00432-021-03843-9. Bcl-2 expression in U251 cells treated with 0, 50 and 100 μM cathepsin inhibitor 1. D-G Analysis of relative expression levels of CTSL, MMP-9 Bax and Bcl-2 in F *P < 0.05 vs. Control group, **P < 0.01 vs. Control group

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