The DOI matches its Crossref record; 44 of the 46 references it cites were found in a registry or an index.
Lipoprotein Lipase Links Dietary Fat to Solid Tumor Cell Proliferation
Open accessPublished version of a preprint
Abstract
Many types of cancer cells require a supply of fatty acids (FA) for growth and survival, and interrupting de novo FA synthesis in model systems causes potent anticancer effects. We hypothesized that, in addition to synthesis, cancer cells may obtain preformed, diet-derived FA by uptake from the bloodstream. This would require hydrolytic release of FA from triglyceride in circulating lipoprotein particles by the secreted enzyme lipoprotein lipase (LPL), and the expression of CD36, the channel for cellular FA uptake. We find that selected breast cancer and sarcoma cells express and secrete active LPL, and all express CD36. We further show that LPL, in the presence of triglyceride-rich lipoproteins, accelerates the growth of these cells. Providing LPL to prostate cancer cells, which express low levels of the enzyme, did not augment growth, but did prevent the cytotoxic effect of FA synthesis inhibition. Moreover, LPL knockdown inhibited HeLa cell growth. In contrast to the cell lines, immunohistochemical analysis confirmed the presence of LPL and CD36 in the majority of breast, liposarcoma, and prostate tumor tissues examined (n = 181). These findings suggest that, in addition to de novo lipogenesis, cancer cells can use LPL and CD36 to acquire FA from the circulation by lipolysis, and this can fuel their growth. Interfering with dietary fat intake, lipolysis, and/or FA uptake will be necessary to target the requirement of cancer cells for FA.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“An elevated expression of lipoprotein lipase (LPL) and monoacylglycerol lipase (MAGL) across diverse cancer subtypes and correlates with invasiveness”
From The emerging hallmarks of cancer metabolism (2016) · cites this paper as Kuemmerle et al., 2011
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Mosmann, T. (1983) · Journal of Immunological Methods · doi:10.1016/0022-1759(83)90303-4 · Cited by 56,104
Cluster analysis and display of genome-wide expression patterns
Eisen, M. B., Spellman, P. T., Brown, P. O., & Botstein, D. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.25.14863 · Cited by 16,184
Sørlie, T., Perou, C. M., Tibshirani, R. J., Aas, T., Geisler, S. B., Johnsen, H., Hastie, T. J., Eisen, M. B., van de Rijn, M., Jeffrey, S. S., et al. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191367098 · Cited by 11,506
Exploration, normalization, and summaries of high density oligonucleotide array probe level data
Irizarry, R. A. (2003) · Biostatistics · doi:10.1093/biostatistics/4.2.249 · Cited by 10,603
Kim, J.-W., Tchernyshyov, I., Semenza, G. L., & Dang, C. V. (2006) · Cell Metabolism · doi:10.1016/j.cmet.2006.02.002 · Cited by 3,905
A collection of breast cancer cell lines for the study of functionally distinct cancer subtypes
Neve, R. M., Chin, K., Fridlyand, J., Yeh, J., Baehner, F. L., Fevr, T., Clark, L., Bayani, N., Coppé, J., Tong, F. K., et al. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.10.008 · Cited by 3,224
Fatty acid synthase and the lipogenic phenotype in cancer pathogenesis
Menendez, J. A., & Lupu, R. (2007) · Nature Reviews Cancer · doi:10.1038/nrc2222 · Cited by 2,941
[19] Receptor-mediated endocytosis of low-density lipoprotein in cultured cells
Goldstein, J. L., Basu, S. K., & Brown, M. S. (1983) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(83)98152-1 · Cited by 1,629
Antioxidant and oncogene rescue of metabolic defects caused by loss of matrix attachment
Schafer, Z. T., Grassian, A. R., Song, L., Jiang, Z., Gerhart-Hines, Z., Irie, H. Y., Gao, S., Puigserver, P., & Brugge, J. S. (2009) · Nature · doi:10.1038/nature08268 · Cited by 1,031
Monoacylglycerol lipase regulates a fatty acid network that promotes cancer pathogenesis
Nomura, D. K., Long, J. Z., Niessen, S., Hoover, H. S., Ng, S.-W., & Cravatt, B. F. (2010) · Cell · doi:10.1016/j.cell.2009.11.027 · Cited by 1,002
Research works printed but not linked: 2
- Weiss, 1986, Fatty-acid biosynthesis in man, a pathway of minor importance, J Biol Chem, 367, 905
- Parlo, 1984, Enhanced rate of citrate export from cholesterol-rich hepatoma mitochondria, J Biol Chem, 259.
Cited by
Sorted by citations
Items 201–287 of 287
Role of Adipose Cells in Tumor Microenvironment
Zhang, T., & Kolonin, M. G. (2013) · Studies in mechanobiology, tissue engineering and biomaterials · doi:10.1007/8415_2013_171 · Cited by 7
Hu, H., Wang, Y., Wang, M., Zhang, Z., Gu, X., Sun, R., Liu, X., Li, N., Ding, N., Li, W., et al. (2025) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.5c01640 · Cited by 6
Metabolomics as a tool for understanding and treating triple-negative breast cancer
Khan, G., Hussain, M. S., Ahmad, S., Alam, N., Ali, S., & Alam, P. (2025) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-025-04234-4 · Cited by 6
Synthesis and fluorine-18 radiolabeling of a phospholipid as a PET imaging agent for prostate cancer
Kwan, K. H., Burvenich, I. J. G., Centenera, M. M., Goh, Y. W., Rigopoulos, A., Dehairs, J., Swinnen, J. V., Raj, G. V., Hoy, A. J., Butler, L. M., et al. (2020) · Nuclear Medicine and Biology · doi:10.1016/j.nucmedbio.2020.11.007 · Cited by 6
β-Estradiol Enhanced Secretion of Lipoprotein Lipase from Mouse Mammary Tumor FM3A Cells
Fujii, T., Ogasawara, M., Kamishikiryo, J., & Morita, T. (2020) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b20-00408 · Cited by 6
Zhai, Q., Luo, M., Zhang, Y., Zhang, W., Wu, C., Lv, S., & Wei, Q. (2022) · Translational Cancer Research · doi:10.21037/tcr-22-431 · Cited by 6
Acidosis Forces Fatty Acid Uptake and Metabolism in Cancer Cells Regardless of Genotype
Ibanez, S., Giolito, M. V., Al‐Siyabi, S., Serafimov, K., Laloux-Morris, F., Dierge, E., Aubert, L., Guilbaud, C., Kaye, S., Rugeles, P. V., et al. (2025) · Advanced Science · doi:10.1002/advs.202505436 · Cited by 5
Yang, R., Han, S., Clayton, J., Haghighatian, M., Tsai, C.-C., Yao, Y., Li, P., Shen, J., & Zhou, Q. Y. (2022) · Cancers · doi:10.3390/cancers14153763 · Cited by 6
Wang, S., Zota, V. E., Vincent, M. Y., Clossey, D., Chen, J., Cieslewicz, M., Watnick, R. S., Mahoney, J., & Watnick, J. (2024) · npj Precision Oncology · doi:10.1038/s41698-024-00774-9 · Cited by 5
Atypical plasma lipid profiles in leukemia
Iqbal, A., Zaid, M., Munir, R., Usman, H., Kalbacher, H., Scandiuzzi, L., & Zaidi, N. (2015) · Clinica Chimica Acta · doi:10.1016/j.cca.2015.11.003 · Cited by 5
Chen, X., Zhu, X., Wei, Z., & Lv, Q. (2019) · Journal of Cellular Biochemistry · doi:10.1002/jcb.29294 · Cited by 5
Catabolic rewiring in cancer impacts dietary interventions
Chinopoulos, C. (2025) · Communications Biology · doi:10.1038/s42003-025-09333-9 · Cited by 6
Association of D4-GDI expression with breast cancer progression
Rosado, L. A. R., Rodriguez‐Canales, J., & Zhang, B. (2012) · Cancer Biomarkers · doi:10.3233/cbm-2012-0240 · Cited by 4
Inaugurating a novel adjuvant therapy in urological cancers: Ferroptosis
Xie, Z., Zhou, Q., Qiu, C., Zhu, D., Li, K., & Huang, H. W. (2022) · Cancer Pathogenesis and Therapy · doi:10.1016/j.cpt.2022.10.002 · Cited by 6
Unravelling the role of obesity and lipids during tumor progression
Zhao, J., Lee, K., Toh, H. C., Lam, K., & Neo, S. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1163160 · Cited by 5
Correlated metabolomic, genomic, and histologic phenotypes in histologically normal breast tissue
Sun, X., Stewart, D. A., Sandhu, R., Kirk, E. L., Pathmasiri, W., McRitchie, S., Clark, R. F., Troester, M. A., & Sumner, S. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193792 · Cited by 4
Knowledge Integration and Representation for Biomedical Analysis
Alachram, H. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8464 · Cited by 4
Grade 4 very severe hypertriglyceridaemia at diagnosis in a child with acute lymphoblastic leukaemia
Khera, S., Kapoor, R., Sunder, S., & Mahajan, D. (2022) · BMJ Case Reports · doi:10.1136/bcr-2021-245820 · Cited by 3
Clinical significance of lipid pathway-targeted therapy in breast cancer
Li, D., Jin, P., Cai, Y., Wu, S., Guo, X., Zhang, Z., Liu, K., Li, P., Hu, Y., & Zhou, Y. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1514811 · Cited by 4
MOREIRA, F. D. S. (2017) · doi:10.47749/t/unicamp.2017.989712 · Cited by 3
Yang, L., Fang, X., Liu, X., Liu, Y., & Zhao, S. (2025) · Tissue and Cell · doi:10.1016/j.tice.2025.103071 · Cited by 2
Li, J., Velaga, R., Takano, Y., & Masuda, N. (2025) · International Journal of Clinical Oncology · doi:10.1007/s10147-025-02916-w · Cited by 2
Nutritional modulation of metabolic signaling within the tumor microenvironment for cancer therapy
Aghdam, M. M., Rezagholizadeh, L., Fazaeli, A., Moradi, A., & Ojarudi, M. (2026) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-025-05462-1 · Cited by 3
Regulation of Lipid Metabolism Under Stress and Its Role in Cancer
Munir, R., & Zaidi, N. (2022) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-031-07634-3_3 · Cited by 3
Cancer Cell Metabolism Featuring Nrf2
Chatterjee, P., Yadav, M., Chauhan, N., Huang, Y. S., & Luo, Y. (2018) · Current Drug Discovery Technologies · doi:10.2174/1570163815666180911092443 · Cited by 2
Metabolic reprogramming and immunity in cancer
Chen, Y., & Li, Y. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-823397-9.00006-5 · Cited by 2
Lipotoxicity as a Barrier for T Cell-Based Therapies
Loschinski, R., Saborido, J. R., Böttcher, M., Kahlfuß, S., & Mougiakakos, D. (2022) · Biomolecules · doi:10.3390/biom12091182 · Cited by 2
Chang, W., Wang, J., You, Y., Wang, H., Xu, S., Vulcano, S., Xu, C., Shen, C., Li, Z., & Wang, J. (2024) · Cancers · doi:10.3390/cancers16030550 · Cited by 1
Walpita, P., Manage, S. A., Gunawardana, D. N., Gunasekara, B., Keerthi, A. A. P., Haputhanthri, P. R., & Perera, M. (2025) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2025.127036 · Cited by 1
The Role of CD36 and Its Regulatory Mechanisms in Metabolic Dysregulation and Tumorigenesis
Tong, C., Feng, W., Yu, H., Liu, Q., Liang, Y., Lan, D., Liu, Q., & Song, B. (2025) · Scandinavian Journal of Immunology · doi:10.1111/sji.70065 · Cited by 2
ANGPTL3, Apo CIII, Leptin and Triglycerides Are Elevated in Metastatic Prostate Cancer
Boulay, G., Khodr, M., Bergeron, A.-C., Chong, E. W., Joncas, F., Castonguay, C., Robitaille, K., Hovington, H., Fradet, V., Bergeron, A., et al. (2026) · Cancers · doi:10.3390/cancers18071176 · Cited by 1
Lipid biomarkers of prostate cancer: insights from triglycerides and saturated fatty acid metabolism
Jx, H., & Li, P. Z. (2026) · Future Oncology · doi:10.1080/14796694.2026.2707002 · Cited by 1
Khan, T. K. (2012) · InTech eBooks · doi:10.5772/2376 · Cited by 1
Fatty acid metabolism related gene MECR contributes to the progression of prostate cancer
Liu, Y., Wan, L., Chen, Y., Zhang, R., Yi, X., Chen, M., Huang, X., & Liu, R. (2025) · Cancer Cell International · doi:10.1186/s12935-025-03738-6 · Cited by 1
Use of X-ray Diffraction Technique of Hair for Oral Cancer Detection: A Proposal
Maniyar, N., & Roopa, N. M. (2019) · The Journal of Contemporary Dental Practice · doi:10.5005/jp-journals-10024-2509 · Cited by 1
EMAP II Expression Is Increased on Peripheral Blood Cells from Non-Hodgkin Lymphoma
Saber, M. M. (2022) · Journal of Immunology Research · doi:10.1155/2022/7219207 · Cited by 1
Yelton, C. J., Yelton, C. J., Kuhn, E. P., Kinlaw, W. B., & Lansigan, F. (2023) · Annals of Clinical Oncology · doi:10.31487/j.aco.2023.01.02 · Cited by 1
Fatty Acid Metabolism as a Potential Therapeutic Target in Thyroid CarcinomaPreprint
Lu, J., Zhang, Y., Sun, M., Ding, C., Zhang, L., Kong, Y., Meng, C. A. I., Miccoli, P., Ma, C., & Yue, X. (2021) · SSRN Electronic Journal · doi:10.2139/ssrn.3861577 · Cited by 1
Kamili, A., & Byrne, J. A. (2014) · Springer eBooks · doi:10.1007/978-81-322-0843-3_11
Adipose and muscle tissue metabolism in cancer cachexia
Agustsson, T. (2011) · Figshare
Investigating Dysregulated Metabolic Pathways that Drive Cancer Pathogenicity
Roberts, L. S. (2017) · eScholarship (California Digital Library)
Metabolic Dysregulation in Environmental Carcinogenesis and Toxicology
Robey, R. B. (2017) · John Wiley & Sons, Inc. eBooks · doi:10.1002/9781119023647.ch15
Mapping Dysregulated Metabolic Pathways in Cancer Using Chemoproteomic and Metabolomic Platforms
Louie, S. M. (2017) · eScholarship (California Digital Library)
Bedewy, A. L., & El-Bendary, W. (2019) · The Egyptian Journal of Haematology · doi:10.4103/ejh.ejh_32_18
Tousignant, K. D. (2020) · Queensland University of Technology · doi:10.5204/thesis.eprints.180822
Mehta, P., Rupala, N., Rawat, S., & Goswami, G. K. (2021) · Indian Journal Of Applied Research · doi:10.36106/ijar/5013991
Fujii, T., Kamishikiryo, J., & Morita, T. (2021) · BPB Reports · doi:10.1248/bpbreports.4.4_130
Chereda, H. (2022) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-9215
The Discovery of Cancer Tissue Specific Proteins in Serum: Case Studies on Prostate Cancer
Spiros, D., & Paul, A. (2012) · InTech eBooks · doi:10.5772/36944
程, 晓. (2022) · Advances in Clinical Medicine · doi:10.12677/acm.2022.1291255
The role of fatty acids metabolism on cancer progression and therapeutics development
Moreira-Barbosa, C., Matos, A., Fernandes, R., Mendes-Ferreira, M., Rodrigues, R. C., Cruz, T., Costa, Â. M., Cardoso, A. P., Ghilardi, C., Oliveira, M. J., et al. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-824043-4.00007-5
Morita, T. (2022) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.22-00098
Rewiring of Drug Metabolism and Its Cross‐talk with Metabolic Reprogramming in Cancer
Majumder, S., & Manna, S. K. (2022) · Wiley eBooks · doi:10.1002/9781119851042.ch27
Cancer and Lipid Metabolism: Roles of Adipocytes on Tumor Microenvironment
Chu, D., Nguyen, Q. H., Le, B. N., Ngoc, S. M. V., Quyen, M. L., & Cao, B. A. (2022) · Springer eBooks · doi:10.1007/978-3-030-80962-1_106-1
Larkin, J. R., Anthony, S. B., Johanssen, V. A., Yeo, T., Sealey, M. A., Yates, A. G., Smith, C. F., Claridge, T. D. W., Nicholson, B. D., Moreland, J., et al. (2023) · doi:10.1158/1078-0432.c.6531243.v1
Gan, X., Cheng, H., Ma, N., Wang, Z., & Mao, Z. (2024) · Research Square · doi:10.21203/rs.3.rs-4929734/v1
Interplay of nutrient stress and lipid dynamics in colorectal cancer cells
Kousar, S., Gull, S., Aqeel, M. B., Shah, F. I., Mahjabeen, I., Shahid, A., Shoaib, N., & Khan, Z. (2025) · Clinical Nutrition Open Science · doi:10.1016/j.nutos.2025.01.005
Vodičková, T., Wozniaková, M., Židlík, V., Žmolíková, J., Dvořáčková, J., Kondé, A., Schwarzerová, J., Grepl, M., & Bouchal, J. (2025) · Biomolecules · doi:10.3390/biom15060758
Altered lipid metabolism and adipocyte activity support HER2+ breast cancer progression
Wong, J. (2017) · Scholars Archive - University at Albany (University at Albany, State University of New York) · doi:10.54014/dvgm-nzy9
Walpita, P., Manage, S. A., Gunawardana, D. N., Gunasekara, B., Punya, K. A. A., Haputhanthri, P. R., & Perera, M. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5352447
Amini, H., Aliabad, H. A. R., Mollania, N., Azadparvar, M., Mollania, F., & Saeed, M. A. (2025) · Optical and Quantum Electronics · doi:10.1007/s11082-025-08389-5
Alshaer, W., Ijjeh, Y., Alsarayreh, N., Alqudah, D. A., Rifai, A., Abu-Siniyeh, A. A., & Alsalem, M. (2025) · Pharmaceutics · doi:10.3390/pharmaceutics17101275
Cancer and Lipid Metabolism: Roles of Adipocytes on Tumor Microenvironment
Chu, D., Nguyen, Q. H., Le, B. N., Ngoc, S. M. V., Quyen, M. L., & Cao, B. A. (2025) · Springer eBooks · doi:10.1007/978-3-032-00761-2_106
Wang, Z., Chao, Z., Wang, Q., Zou, F., Song, T., Xu, L., Ning, J., & Cheng, F. (2024) · Figshare · doi:10.6084/m9.figshare.26673225
Tobin, A. J., Noel, N. P., Christian, S. L., & Brown, R. (2021) · Figshare · doi:10.6084/m9.figshare.15184794
Tobin, A. J., Noel, N. P., Christian, S. L., & Brown, R. (2021) · Figshare · doi:10.6084/m9.figshare.15184800
Wang, Z., Chao, Z., Wang, Q., Zou, F., Song, T., Xu, L., Ning, J., & Cheng, F. (2024) · Figshare · doi:10.6084/m9.figshare.26673231
Wang, Z., Chao, Z., Wang, Q., Zou, F., Song, T., Xu, L., Ning, J., & Cheng, F. (2024) · Figshare · doi:10.6084/m9.figshare.26673228
Chereda, H., Bleckmann, A., Menck, K., Perera-Bel, J., Stegmaier, P., Auer, F., Krämer, F., Leha, A., & Beißbarth, T. (2021) · Figshare · doi:10.6084/m9.figshare.14205239
Wang, Z., Chao, Z., Wang, Q., Zou, F., Song, T., Xu, L., Ning, J., & Cheng, F. (2024) · Figshare · doi:10.6084/m9.figshare.26673219
Tobin, A. J., Noel, N. P., Christian, S. L., & Brown, R. (2021) · Figshare · doi:10.6084/m9.figshare.15184803
Wang, Z., Chao, Z., Wang, Q., Zou, F., Song, T., Xu, L., Ning, J., & Cheng, F. (2024) · Figshare · doi:10.6084/m9.figshare.26673234
Tobin, A. J., Noel, N. P., Christian, S. L., & Brown, R. (2021) · Figshare · doi:10.6084/m9.figshare.15184806
Wang, Z., Chao, Z., Wang, Q., Zou, F., Song, T., Xu, L., Ning, J., & Cheng, F. (2024) · Figshare · doi:10.6084/m9.figshare.26673222
Kaminski, L. (2018) · theses.fr (ABES) · doi:10.70675/7f6ae88bz4f3cz49d3zafcdz8682254b2be3
Bousset, L. (2019) · theses.fr (ABES) · doi:10.70675/45b0b676z18daz47a9zbb03zee607f300175
Targeting the metabolic environment to modulate T cell effector function
Matias, M. I. (2019) · theses.fr (ABES) · doi:10.70675/0582ddaaze61dz4707z9cb1zdb8fe1d82653
Vaishnavi, M., Kumari, M., Pal, S., Kaur, K., Kaity, S., Mandal, C., & Roy, S. (2026) · In vitro models · doi:10.1007/s44164-026-00119-9
Narasimhan, A., Cheung, C. W., Kajabadi, N., Lin, B., Tung, L. W., Chang, C., & Rossi, F. M. V. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117362 · Cited by 1
Guo, Y.-J., Zhao, R., Li, Y. Q., Cui, J.-J., Zhao, M.-R., Yang, Y., Wu, J.-Y., Zhao, J.-H., & Song, X. (2026) · Cellular Signalling · doi:10.1016/j.cellsig.2026.112722
Ye, F., Wu, J., Liu, D., 李俞慧, Zhu, N., & Chen, L. (2026) · Cellular Signalling · doi:10.1016/j.cellsig.2026.112911
Metadata
- Authors
- Kuemmerle, N. B., Rysman, E., Lombardo, P. S., Flanagan, A. J., Lipe, B. C., Wells, W. A., Pettus, J. R., Froehlich, H. M., Memoli, V. A., Morganelli, P. M., Swinnen, J. V., Timmerman, L. A., Chaychi, L., Fricano, C. J., Eisenberg, B. L., Coleman, W. B., & Kinlaw, W. B.
- Affiliations
- Dartmouth–Hitchcock Medical Center (US)
- University of North Carolina at Chapel Hill (US)
- Corresponding author
- Kinlaw, William B.
- ORCID
- Venue
- Molecular Cancer Therapeutics
- Published
- 2011-03-01
- Volume
- 10
- Issue
- 3
- Pages
- 427-436
- ISSN
- 1535-7163 (ISSN-L)
- 1538-8514
- PMC
- PMC3074101
- OpenAlex
- W2117594441
- Cited by
- 286
- References
- 46
- Citations by year
- 2026: 7 · 2025: 18 · 2024: 22 · 2023: 20 · 2022: 31 · 2021: 35 · 2020: 24 · 2019: 32 · 2018: 19 · 2017: 16 · 2016: 21 · 2015: 11 · 2014: 9 · 2013: 8 · 2012: 11
- FWCI
- 3.26
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Molecular Cancer Therapeutics (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Carolina Digital Repository (University of North Carolina at Chapel Hill) (submittedVersion)
- UNC Libraries
- Funders
- Howard Hughes Medical Institute (52005870)
- Dartmouth College
- Fonds Wetenschappelijk Onderzoek
- Universität Ulm
- Vlaamse regering
- Norris Cotton Cancer Center
- National Cancer Institute (R01CA126618, P50CA058207, P30CA023108)
- National Institute of Diabetes and Digestive and Kidney Diseases (T32DK007508, DK 07508)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Lipids, and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Keywords
- lipoprotein lipase, CD36, fatty acid uptake, dietary fat, solid tumor growth, lipolysis, triglyceride-rich lipoproteins, breast cancer, sarcoma, prostate cancer, fatty acid synthesis inhibition, cancer metabolism
- MeSH terms
- Animals, Dietary Fats, Fatty Acids, Female, Humans, Lipolysis, Lipoprotein Lipase, Liposarcoma, Male, Mice, Transgenic, Neoplasms, CD36 Antigens, Oligonucleotide Array Sequence Analysis, RNA, Small Interfering, Cell Line, Tumor, Cell Proliferation, Mice, Fatty Acid Synthesis Inhibitors
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review