Autophagy and Tumor Metabolism

Repertoires of Autophagy in the Pathogenesis of Ocular Diseases

Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351

Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation

Vander Heiden, M. G., Cantley, L. C., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1160809 · Cited by 16,197

The emerging hallmarks of cancer metabolism

Pavlova, N. N., & Thompson, C. B. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2015.12.006 · Cited by 5,926 · cited 1×

Autophagy: process and functionPreprint

Mizushima, N. (2007) · Genes & Development · doi:10.1101/gad.1599207 · Cited by 4,104

Development by Self-Digestion

Levine, B., & Klionsky, D. J. (2004) · Developmental Cell · doi:10.1016/s1534-5807(04)00099-1 · Cited by 3,728

Induction of autophagy and inhibition of tumorigenesis by beclin 1

Liang, X. H., Jackson, S., Seaman, M., Brown, K., Kempkes, B., Hibshoosh, H., & Levine, B. (1999) · Nature · doi:10.1038/45257 · Cited by 3,347

The AMPK signalling pathway coordinates cell growth, autophagy and metabolism

Mihaylova, M. M., & Shaw, R. J. (2011) · Nature Cell Biology · doi:10.1038/ncb2329 · Cited by 2,923

Understanding the Intersections between Metabolism and Cancer Biology

Heiden, M. G. V., & DeBerardinis, R. J. (2017) · Cell · doi:10.1016/j.cell.2016.12.039 · Cited by 2,369

Promotion of tumorigenesis by heterozygous disruption of the beclin 1 autophagy gene

Qu, X., Yu, J., Bhagat, G., Furuya, N., Hibshoosh, H., Troxel, A., Rosen, J., Eskelinen, E.-L., Mizushima, N., Ohsumi, Y., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci20039 · Cited by 2,311

MTOR: a pharmacologic target for autophagy regulation

Kim, Y. C., & Guan, K.-L. (2015) · Journal of Clinical Investigation · doi:10.1172/jci73939 · Cited by 2,126

Epigenetic silencing of miR-342-3p in B cell lymphoma and its impact on autophagy

Zhang, M. Y., Călin, G. A., Yuen, K., Jin, D., & Chim, C. S. (2020) · Clinical Epigenetics · doi:10.1186/s13148-020-00926-1 · Cited by 21

The Anti-Tumor Effect and Mechanism of Triterpenoids in Rhus chinensis Mill. on Reversing Effector CD8+ T-cells Dysfunction by Targeting Glycolysis Pathways in Colorectal Cancer

Wang, G., Wang, Y.-Z., Yu, Y., Yin, P., Xu, K., & Zhang, H. (2021) · Integrative Cancer Therapies · doi:10.1177/15347354211017219 · Cited by 22

Optimization of Beclin 1-Targeting Stapled Peptides by Staple Scanning Leads to Enhanced Antiproliferative Potency in Cancer Cells

Yang, Q., Qiu, X., Zhang, X., Yu, Y., Li, N., Wei, X., Feng, G., Li, Y., Zhao, Y., & Wang, R. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.1c00870 · Cited by 21

Fucoidan as an Autophagy Regulator: Mechanisms and Therapeutic Potentials for Cancer and Other Diseases

Zhang, N., Xue, M., Sun, T., Yang, J., Pei, Z., & Qin, K. (2021) · Nutrition and Cancer · doi:10.1080/01635581.2021.1973045 · Cited by 21

Overexpression of circCDR1as drives oral squamous cell carcinoma progression

Cui, L., Huang, C., & Zhou, D. Y. (2021) · Oral Diseases · doi:10.1111/odi.14085 · Cited by 20

Autophagy, molecular chaperones, and unfolded protein response as promoters of tumor recurrence

Alhasan, B. A., Mikeladze, M. A., Guzhova, I. V., & Margulis, B. A. (2023) · Cancer and Metastasis Reviews · doi:10.1007/s10555-023-10085-3 · Cited by 20

A minimalist dendrimer nanodrug for autophagy inhibition-amplified tumor photothermo-immunotherapy

Ouyang, Z., Gao, Y., Shen, S., Jia, B., Yu, H., Wang, H., Shen, M., & Shi, X. (2023) · Nano Today · doi:10.1016/j.nantod.2023.101936 · Cited by 21

Regulation of mitochondrial metabolism by autophagy supports leptin-induced cell migration

García-Miranda, A., Montes-Alvarado, J. B., Sarmiento-Salinas, F. L., Vallejo‐Ruiz, V., Castañeda-Saucedo, E., Navarro‐Tito, N., & Maycotte, P. (2024) · Scientific Reports · doi:10.1038/s41598-024-51406-y · Cited by 22

Nanoplatform-based strategies for enhancing the lethality of current antitumor PDT

Lu, X., Xue, C., Dong, J., Zhang, Y., & Gao, F. (2024) · Journal of Materials Chemistry B · doi:10.1039/d4tb00008k · Cited by 22

A Comparative Analysis of the Anti-Tumor Activity of Sixteen Polysaccharide Fractions from Three Large Brown Seaweed, Sargassum horneri, Scytosiphon lomentaria, and Undaria pinnatifida

Song, L., Niu, Y., Chen, R., Ju, H., Liu, Z., Zhang, B., Xie, W., & Gao, Y. (2024) · Marine Drugs · doi:10.3390/md22070316 · Cited by 20

The autophagy scaffold protein ALFY is critical for the granulocytic differentiation of AML cells

Schläfli, A. M., Isakson, P., Garattini, E., Simonsen, A., & Tschan, M. P. (2017) · Scientific Reports · doi:10.1038/s41598-017-12734-4 · Cited by 21

2-Aminoethoxydiphenylborane sensitizes anti-tumor effect of bortezomib via suppression of calcium-mediated autophagy

Qu, Y. Q., Gordillo-Martínez, F., Law, B. Y. K., Han, Y. K., Wu, A., Wu, J., Lam, W. K., Ho, C., Mok, S. W. F., He, H. Q., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-0397-0 · Cited by 21

PIM kinase inhibitor, AZD1208, inhibits protein translation and induces autophagy in primary chronic lymphocytic leukemia cells

Cervantes-Gomez, F., Stellrecht, C. M., Ayres, M., Keating, M. J., Wierda, W. G., & Gandhi, V. V. (2019) · Oncotarget · doi:10.18632/oncotarget.26876 · Cited by 20

Xenophagy in cancer

Ammanathan, V., Vats, S., Abraham, I. M., & Manjithaya, R. R. (2020) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2020.02.015 · Cited by 21

Sanguisorba officinalis L. Suppresses Triple-Negative Breast Cancer Metastasis by Inhibiting Late-Phase Autophagy via Hif-1α/Caveolin-1 Signaling

Wang, N., Muhetaer, G., Zhang, X., Yang, B., Wang, C., Zhang, Y., Wang, X., Zhang, J., Wang, S., Zheng, Y., et al. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.591400 · Cited by 20

Role of the USP family in autophagy regulation and cancer progression

Liu, C., Yuan, Y., Zhan, Y., Zou, M., Wu, L., Zhang, C., Chen, B., Zeng, H., Yang, R., Hu, T., et al. (2025) · APOPTOSIS · doi:10.1007/s10495-025-02095-z · Cited by 21

Click-Nucleic-Acid-Containing Codelivery System Inducing Collapse of Cellular Homeostasis for Tumor Therapy through Bidirectional Regulation of Autophagy and Glycolysis

Guo, Q., Chen, Q., Zhang, Y., Zhou, W., Li, X., Li, C., Zhang, Y., Chen, H., Liu, P., Chu, Y., et al. (2020) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.0c18361 · Cited by 19

LACTB induced apoptosis of oxaliplatin-resistant gastric cancer through regulating autophagy-mediated mitochondrial apoptosis pathway.

Yang, F., Yan, Z., Nie, W., Cheng, X., Liu, Z., Wang, W., Shao, C., Fu, G., & Yu, Y. (2021) · PubMed · Cited by 20

Development and Validation of an Autophagy-Related LncRNA Prognostic Signature in Head and Neck Squamous Cell Carcinoma

Shen, L., Li, N., Zhou, Q. C., Li, Z., & Shen, L. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.743611 · Cited by 19

X-ray cross-complementing family: the bridge linking DNA damage repair and cancer

Liu, Q., Qiu, P., Zhang, B., & Tan, Y. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04447-2 · Cited by 30

Multifunctional fluorescent probes "killing two birds with one stone" - recent progress and outlook

Qi, Y., Chen, L., Guo, L., Cao, Y., Wang, H., Yang, Y., Lu, Y., & Zhu, H. (2020) · Applied Materials Today · doi:10.1016/j.apmt.2020.100877 · Cited by 20

PAX5-activated lncRNA ARRDC1-AS1 accelerates the autophagy and progression of DLBCL through sponging miR-2355-5p to regulate ATG5

Xu, H., Yu, X., Yang, Z., Song, Q., Cheng, S., He, Z., & Dai, L. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119932 · Cited by 19

Regulation of autophagy as a therapeutic option in glioblastoma

Manea, A. J., & Ray, S. K. (2021) · APOPTOSIS · doi:10.1007/s10495-021-01691-z · Cited by 20

Molecular Pathway Analysis Indicates a Distinct Metabolic Phenotype in Women With Right-Sided Colon Cancer

Sun, Y., Mironova, V., Chen, Y., Lundh, E. P. F., Zhang, Q., Cai, Y. A., Vasiliou, V., Zhang, Y., García-Milian, R., Khan, S. A., et al. (2019) · Translational Oncology · doi:10.1016/j.tranon.2019.09.004 · Cited by 18

Construction and Validation of an Autophagy-Related Prognostic Risk Signature for Survival Predicting in Clear Cell Renal Cell Carcinoma Patients

Yang, H., Han, M., & Li, H. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.00707 · Cited by 18

A Novel Six-Gene-Based Prognostic Model Predicts Survival and Clinical Risk Score for Gastric Cancer

Li, J., Pu, K., Li, C., Wang, Y., & Zhou, Y. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.615834 · Cited by 18

SLC45A4 promotes glycolysis and prevents AMPK/ULK1‐induced autophagy in TP53 mutant pancreatic ductal adenocarcinoma

Chen, W., Huang, F., Huang, J., Li, Y., Peng, J., Zhuang, Y., Huang, X., Lu, L., Zhu, Z., & Zhang, S. (2021) · The Journal of Gene Medicine · doi:10.1002/jgm.3364 · Cited by 19

AMPK-Mediated Metabolic Switching Is High Effective for Phytochemical Levo-Tetrahydropalmatine (l-THP) to Reduce Hepatocellular Carcinoma Tumor Growth

Yin, X., Li, W., Zhang, J., Zhao, W., Cai, H., Zhang, C., Liu, Z., Guo, Y. P., & Wang, J. (2021) · Metabolites · doi:10.3390/metabo11120811 · Cited by 18

TBC1D14 inhibits autophagy to suppress lymph node metastasis in head and neck squamous cell carcinoma by downregulating macrophage erythroblast attacher

Lu, T., Li, Y., Pan, M., Yu, D. B., Wang, Z., Liu, C., & Hu, G. (2022) · International Journal of Biological Sciences · doi:10.7150/ijbs.68992 · Cited by 18

Autophagy in PDGFRα+ mesenchymal cells is essential for intestinal stem cell survival

Yang, Y., Gomez-Jenkins, M., Marsh, T., Poillet-Perez, L., Sawant, A., Chen, L., Park, N. R., Jackson, S. R., Hu, Z. S., Alon, N., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2202016119 · Cited by 21

Inhibition of hypoxia‐induced HIF‐1α‐mediated autophagy enhances the in vitro antitumor activity of rhein in pancreatic cancer cells

Yao, C., & Wang, F. (2022) · Journal of Applied Toxicology · doi:10.1002/jat.4365 · Cited by 18

NRBF2-mediated autophagy contributes to metabolite replenishment and radioresistance in glioblastoma

Kim, J., Kang, H., Son, B., Kim, M., Kang, J., Park, K. H., Jeon, J., Jo, S., Kim, H. Y., Youn, H., et al. (2022) · Experimental & Molecular Medicine · doi:10.1038/s12276-022-00873-2 · Cited by 18

Autophagy, a critical element in the aging male reproductive disorders and prostate cancer: a therapeutic point of view

Raee, P., Tan, S. C., Najafi, S., Zandsalimi, F., Low, T. Y., Aghamiri, S., Fazeli, E., Aghapour, M., Mofarahe, Z. S., Heidari, M. H., et al. (2023) · Reproductive Biology and Endocrinology · doi:10.1186/s12958-023-01134-1 · Cited by 18

Bisabosqual A: A novel asparagine synthetase inhibitor suppressing the proliferation and migration of human non-small cell lung cancer A549 cells

Pan, Y., Suzuki, T., Sakai, K., Hirano, Y., Ikeda, H., Hattori, A., Dohmae, N., Nishio, K., & Kakeya, H. (2023) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2023.176156 · Cited by 18

Inhibition of IRP2-dependent reprogramming of iron metabolism suppresses tumor growth in colorectal cancer

Hwang, J., Park, A., Kim, C., Kim, C. G., Kwak, J., Kim, B., Shin, H., Ku, M., Yang, J., Baek, A., et al. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01769-6 · Cited by 19

From Molecular Therapies to Lysosomal Transplantation and Targeted Drug Strategies: Present Applications, Limitations, and Future Prospects of Lysosomal Medications

Alhowyan, A., & Harisa, G. I. (2025) · Biomolecules · doi:10.3390/biom15030327 · Cited by 19

Autophagy in the mammalian nervous system: a primer for neuroscientists

Suomi, F., & McWilliams, T. G. (2019) · Neuronal Signaling · doi:10.1042/ns20180134 · Cited by 18

Reduced expression of proteolipid protein 2 increases ER stress‐induced apoptosis and autophagy in glioblastoma

Feng, Z., Zhou, W., Wang, J., Qi, Q., Han, M., Kong, Y., Hu, Y., Zhang, Y., Chen, A., Huang, B., et al. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14840 · Cited by 18

Cadmium induces cell growth in A549 and HELF cells via autophagy-dependent glycolysis

Wang, X., Li, Z., Gao, Z., Li, Q., Jiang, L., Geng, C., Yao, X., Shi, X., Liu, Y., & Cao, J. (2020) · Toxicology in Vitro · doi:10.1016/j.tiv.2020.104834 · Cited by 18

Overexpression of ATG4a promotes autophagy and proliferation, and inhibits apoptosis in lens epithelial cells via the AMPK and Akt pathways

Yan, C., Zhao, J., Yu, Q., Zhao, F., Ji, L., & Zhang, J. (2020) · Molecular Medicine Reports · doi:10.3892/mmr.2020.11205 · Cited by 18

A Risk Signature with Autophagy-Related Long Noncoding RNAs for Predicting the Prognosis of Clear Cell Renal Cell Carcinoma: Based on the TCGA Database and Bioinformatics

Xuan, Y., Chen, W., Liu, K., Gao, Y., Zuo, S., Wang, B., Ma, X., & Zhang, X. (2021) · Disease Markers · doi:10.1155/2021/8849977 · Cited by 18

Targeting extracellular matrix interaction in gastrointestinal cancer: Immune modulation, metabolic reprogramming, and therapeutic strategies

Li, J., Zhang, W., Chen, L., Wang, X., Liu, J., Huang, Y., Qi, H., Chen, L., Wang, T., & Li, Q. (2024) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2024.189225 · Cited by 18

P53-regulated autophagy and its impact on drug resistance and cell fate

Shim, D. (2021) · Cancer Drug Resistance · doi:10.20517/cdr.2020.85 · Cited by 20

Synergistic combination of cytotoxic chemotherapy and cyclin‐dependent kinase 4/6 inhibitors in biliary tract cancers

Arora, M., Bogenberger, J. M., Abdelrahman, A. M., Yonkus, J. A., Alva‐Ruiz, R., Leiting, J. L., Chen, X., Usón, P. L. S., Dumbauld, C., Baker, A. T., et al. (2021) · Hepatology · doi:10.1002/hep.32102 · Cited by 17

ER-phagy in the Occurrence and Development of Cancer

Zhou, H., Wang, K., Wang, M., Zhao, W., Zhang, C.-H., Cai, M., Qiu, Y., Zhang, T., Shao, R., & Zhao, W. (2022) · Biomedicines · doi:10.3390/biomedicines10030707 · Cited by 18

The functions and roles of C2H2 zinc finger proteins in hepatocellular carcinoma

Li, Q., Guoqian, T., & Wu, F. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1129889 · Cited by 17

Integrated transcriptomic and metabolomic analysis reveals the metabolic programming of GM-CSF- and M-CSF- differentiated mouse macrophages

Zhang, Q., Song, Q., Liu, S., Xu, Y., Gao, D., Lu, P., Liu, Y.-T., Zhao, G., Wu, L., Zhao, C., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1230772 · Cited by 18

Exploring the potential of asparagine restriction in solid cancer treatment: recent discoveries, therapeutic implications, and challenges

Fontes, M. G., Silva, C., Roldán, W. H., & Monteiro, G. (2024) · Medical Oncology · doi:10.1007/s12032-024-02424-3 · Cited by 18

TNKS1BP1 facilitates ubiquitination of CNOT4 by TRIM21 to promote hepatocellular carcinoma progression and immune evasion

Wang, Y., Sandrine, I. K., Ma, L., Chen, K., Chen, X., Yu, Y., Wang, S., Xiao, L., Li, C., Liu, Y., et al. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06897-y · Cited by 17

Degradation of p47 by autophagy contributes to CADM1 overexpression in ATLL cells through the activation of NF-κB

Sarkar, B., Nishikata, I., Nakahata, S., Ichikawa, T., Shiraga, T., Saha, H. R., Fujii, M., Tanaka, Y., Shimoda, K., & Morishita, K. (2019) · Scientific Reports · doi:10.1038/s41598-019-39424-7 · Cited by 17

Current Status and Future Prospects of Clinically Exploiting Cancer-specific Metabolism—Why Is Tumor Metabolism Not More Extensively Translated into Clinical Targets and Biomarkers?

Muthu, M., & Nordström, A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20061385 · Cited by 16

Circular RNAs in gastric cancer: Biomarkers for early diagnosis (Review)

Yang, C., Qiao, G., Song, L., Bao, S., & Ma, L. (2020) · Oncology Letters · doi:10.3892/ol.2020.11623 · Cited by 17

A novel potent autophagy inhibitor ECDD-S27 targets vacuolar ATPase and inhibits cancer cell survival

Paha, J., Kanjanasirirat, P., Munyoo, B., Tuchinda, P., Suvannang, N., Nantasenamat, C., Boonyarattanakalin, K., Kittakoop, P., Srikor, S., Kongklad, G., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-45641-x · Cited by 17

Discovery of Fused Benzimidazole-Imidazole Autophagic Flux Inhibitors for Treatment of Triple-Negative Breast Cancer

Yang, D., Zhang, Y., Lei, J., Li, S., He, L., Tang, D., Xu, C. S., Zhang, L., Wen, J., Lin, H., et al. (2022) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2022.114565 · Cited by 16

Pancreatic ductal adenocarcinoma: Emerging therapeutic strategies

Osei‐Bordom, D., Serifis, N., Brown, Z. J., Hewitt, D. B., Lawal, G., Sachdeva, G. S., Cloonan, D. J., & Pawlik, T. M. (2022) · Surgical Oncology · doi:10.1016/j.suronc.2022.101803 · Cited by 17

Crosstalk of renal cell carcinoma cells and tumor-associated macrophages aggravates tumor progression by modulating muscleblind-like protein 2/B-cell lymphoma 2/beclin 1-mediated autophagy

He, C., Li, Y., Chen, Z., & Huang, C. (2022) · Cytotherapy · doi:10.1016/j.jcyt.2022.09.001 · Cited by 16

Co-Targeting the EGFR and PI3K/Akt Pathway to Overcome Therapeutic Resistance in Head and Neck Squamous Cell Carcinoma: What about Autophagy?

Zaryouh, H., Loenhout, J. V., Peeters, M., Vermorken, J. B., Lardon, F., & Wouters, A. (2022) · Cancers · doi:10.3390/cancers14246128 · Cited by 16

Epigenetic modification and exosome effects on autophagy in osteoarthritis

Cheng, C., Wu, Y., Huang, Y., Xue, Q., Wang, Y., Liao, F., Wang, X., & Miao, C. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115930 · Cited by 16

DIRAS3 induces autophagy and enhances sensitivity to anti-autophagic therapy in KRAS-driven pancreatic and ovarian carcinomas

Bildik, G., Gray, J. P., Mao, W., Yang, H., Özyurt, R., Orellana, V. R., Wever, O. D., Carey, M. S., Bast, R. C., & Lü, Z. (2024) · Autophagy · doi:10.1080/15548627.2023.2299516 · Cited by 16

Platycodin D induces apoptosis via regulating MAPK pathway and promotes autophagy in colon cancer cell

Han, S., Lee, J.-H., Woo, J., Jung, G.-H., Jung, S., Han, E.-J., Park, Y., Kim, B.-S., Kim, S., Park, B.-K., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116216 · Cited by 18

New insights into the roles of lactylation in cancer

Zhu, Y. E., Liu, W., Luo, Z., Xiao, F., & Sun, B. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1412672 · Cited by 16

Inhibitory effects of 5-heptadecylresorcinol on the proliferation of human MCF-7 breast cancer cells through modulating PI3K/Akt/mTOR pathway

Xie, M., Liu, J., Wang, Z., Sun, B., & Wang, J. (2020) · Journal of Functional Foods · doi:10.1016/j.jff.2020.103946 · Cited by 16

Autophagy-related long noncoding RNAs can predict prognosis in patients with bladder cancer

Lai, C., Wu, Z., Shi, J., Li, K., Zhu, J., Chen, Z., Liu, C., & Xu, K. (2020) · Aging · doi:10.18632/aging.103947 · Cited by 16

The Role and Mechanism of ATM-Mediated Autophagy in the Transition From Hyper-Radiosensitivity to Induced Radioresistance in Lung Cancer Under Low-Dose Radiation

Wang, Q., Chen, Y., Chang, H., Hu, T., Wang, J., Xie, Y., & Cheng, J. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.650819 · Cited by 16

Comparing the Secretomes of Chemorefractory and Chemoresistant Ovarian Cancer Cell Populations

Lee, A. H., Peña, C. M., & Dawson, M. (2022) · Cancers · doi:10.3390/cancers14061418 · Cited by 17

Advanced Bioinformatics Analysis and Genetic Technologies for Targeting Autophagy in Glioblastoma Multiforme

Manea, A. J., & Ray, S. K. (2023) · Cells · doi:10.3390/cells12060897 · Cited by 17

Novel Carrier-Free Nanodrug Enhances Photodynamic Effects by Blocking the Autophagy Pathway and Synergistically Triggers Immunogenic Cell Death for the Efficient Treatment of Breast Cancer

Xie, L., Wang, L., Li, L., Liu, C., Guo, L., Liao, Y., Zhou, S., Wu, W., Duo, Y., Shi, L., et al. (2024) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.3c17977 · Cited by 15

Advances in herbal polysaccharides-based nano-drug delivery systems for cancer immunotherapy

Han, M., Fan, Y.-K., Zhang, Y., & Dong, Z. (2024) · Journal of drug targeting · doi:10.1080/1061186x.2024.2309661 · Cited by 15

Activated hepatic stellate cells promote progression of post-heat residual hepatocellular carcinoma from autophagic survival to proliferation

Zhang, R., Lin, X., Liu, H., Ma, M., Chen, J., Chen, J., Gao, D., Cui, J., & Chen, R. (2019) · International Journal of Hyperthermia · doi:10.1080/02656736.2018.1558459 · Cited by 15

CDK5RAP3 Participates in Autophagy Regulation and Is Downregulated in Renal Cancer

Li, J., Hu, X., Su, M., Shen, H., Qiu, W., & Tian, Y. (2019) · Disease Markers · doi:10.1155/2019/6171782 · Cited by 15

FOXK2 promotes the proliferation of papillary thyroid cancer cell by down-regulating autophagy

Li, S., Wang, P., Ju, H., Zhu, T., Shi, J., & Huang, Y. (2022) · Journal of Cancer · doi:10.7150/jca.60730 · Cited by 15

Autophagy-Associated Immunogenic Modulation and Its Applications in Cancer Therapy

Duan, Z., Shi, Y., Lin, Q., Hamaï, A., Mehrpour, M., & Gong, C. (2022) · Cells · doi:10.3390/cells11152324 · Cited by 16

Identification of Autophagy-Related LncRNA to Predict the Prognosis of Colorectal Cancer

Duan, L., Yang, X., Li, C., Lan, N., & Hou, X. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.906900 · Cited by 15

Icariin inhibits autophagy and promotes apoptosis in SKVCR cells through mTOR signal pathway

Jiang, S., Chang, H., Deng, S., & Fan, D. (2018) · Cellular and Molecular Biology · doi:10.14715/cmb/2018.64.6.2 · Cited by 15

Macropinocytosis Fuels Prostate Cancer

Commisso, C., & Debnath, J. (2018) · Cancer Discovery · doi:10.1158/2159-8290.cd-18-0513 · Cited by 16

CD44 Receptor–Specific and Redox-Sensitive Nanophotosensitizers of Hyaluronic Acid–Chlorin e6 Tetramer Having Diselenide Linkages for Photodynamic Treatment of Cancer Cells

Kim, D.-M., Shim, Y., Kwon, H., Kim, J., Park, J.-I., Kim, D.-H., Kim, J. H., Kim, J. H., & Jeong, Y. (2019) · Journal of Pharmaceutical Sciences · doi:10.1016/j.xphs.2019.07.024 · Cited by 15

Rhodiola crenulata extract decreases fatty acid oxidation and autophagy to ameliorate pulmonary arterial hypertension by targeting inhibition of acylcarnitine in rats

Ren, H., Zheng, N. I. U., Guo, R., Fu, M., Li, H., ZHANG, X.-Y., & Li, Y. (2021) · Chinese Journal of Natural Medicines · doi:10.1016/s1875-5364(21)60013-4 · Cited by 14

Degradative and Non-Degradative Roles of Autophagy Proteins in Metabolism and Metabolic Diseases

Kuramoto, K., & He, C. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.844481 · Cited by 16

Comprehensive analysis of autophagy related long non-coding RNAs in prognosis, immunity, and treatment of muscular invasive bladder cancer

Tan, W., Yuan, Y., Huang, H., Ma, J., Li, Y., Gou, Y., Wu, H., & Hu, Z. (2022) · Scientific Reports · doi:10.1038/s41598-022-13952-1 · Cited by 14

Gankyrin and TIGAR cooperatively accelerate glucose metabolism toward the PPP and TCA cycle in hepatocellular carcinoma

Yang, C., Cui, X., Ding, Z., Jiang, T., Feng, X., Pan, Y., Lin, Y., Shang, T., Wang, Q., Pan, J., et al. (2022) · Cancer Science · doi:10.1111/cas.15593 · Cited by 14

Non-canonical autophagy in aging and age-related diseases

Kumar, A. V., & Mills, J. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1137870 · Cited by 15

Unravelling the complexity of lncRNAs in autophagy to improve potential cancer therapy

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