Relevant bibliographies by topics / Anticancer MCF-7

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Anticancer MCF-7'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Anticancer MCF-7"

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Devi, Senthil, Velliyagounder Venkateswaran, and Kanakaraj Lakshmi. "Cytotoxic evaluation of curcumin and quercetin in MCF-7 cell lines." World Journal of Biology Pharmacy and Health Sciences 17, no. 2 (2024): 149–54. https://doi.org/10.5281/zenodo.11283598.

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Cytotoxic evaluation of Curcumin and Quercetin in MCF-7 cell lines was performed to assess their potential anticancer activity. MCF-7 is a widely used breast cancer cell line, and evaluating the cytotoxic effects of the compounds on these cells can provide valuable information about their potential as an anticancer agent. Curcumin, a naturally occurring compound found in turmeric, has been extensively studied for its potential anticancer properties, including its effects on MCF-7 cell lines. MCF-7 cells are commonly used as a model for studying breast cancer. Quercetin, a flavonoid found in va
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Devi Senthil, Venkateswaran Velliyagounder, and Lakshmi Kanakaraj. "Cytotoxic evaluation of curcumin and quercetin in MCF-7 cell lines." World Journal of Biology Pharmacy and Health Sciences 17, no. 2 (2024): 149–54. http://dx.doi.org/10.30574/wjbphs.2024.17.2.0048.

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Cytotoxic evaluation of Curcumin and Quercetin in MCF-7 cell lines was performed to assess their potential anticancer activity. MCF-7 is a widely used breast cancer cell line, and evaluating the cytotoxic effects of the compounds on these cells can provide valuable information about their potential as an anticancer agent. Curcumin, a naturally occurring compound found in turmeric, has been extensively studied for its potential anticancer properties, including its effects on MCF-7 cell lines. MCF-7 cells are commonly used as a model for studying breast cancer. Quercetin, a flavonoid found in va
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Wang, Li-Ping, Zhi Xu, Gui-Ying Deng, and Sha-Li Xu. "Antiproliferative Activity of 8-methoxy Ciprofloxacin-Hydrozone/Acylhydrazone Scaffolds." Current Topics in Medicinal Chemistry 20, no. 21 (2020): 1911–15. http://dx.doi.org/10.2174/1568026620666200603105644.

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Aims: A series of 8-methoxy ciprofloxacin- hydrazone/acylhydrazone hybrids were evaluated for their activity against a panel of cancer cell lines including HepG2 liver cancer cells, MCF-7, doxorubicin- resistant MCF-7 (MCF-7/DOX) breast cancer cells, DU-145 and multidrug-resistant DU145 (MDR DU-145) prostate cancer cells to seek for novel anticancer agents. Background: Ciprofloxacin with excellent pharmacokinetic properties as well as few side effects, is one of the most common used antibacterial agents. Notably, Ciprofloxacin could induce cancer cells apoptosis, and cell cycle arrest at the S
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Salman, Husam Hamza, Munther Abduljaleel Mohammed Ali, and Eman Tariq Ali. "Synthesis and screening of anticancer potentials of some new terephthaldehyde-derived nitrone compounds." Tropical Journal of Pharmaceutical Research 19, no. 2 (2020): 341–49. http://dx.doi.org/10.4314/tjpr.v19i2.17.

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Purpose: To synthesize and screen some new nitrone compounds derived from terephthaldehyde for their anticancer potential.
 Methods: Six new compounds (H, p-Me,p-Br, p-Cl, o-Cl and m-Me) were synthesized via a condensation reaction between terephthaldehyde and a variety of aryl hydroxylamine compounds derived from nitrobenzene and its derivatives. The chemical structures of these compounds were identified using elemental CHN analysis and were elucidated using Fourier Transform infra-red (FT-IR), 1H-nuclear magnetic resonance (1H NMR), mass spectrometry (MS), and elemental analysis. The an
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Achakzai, Jahangir Khan, Muhammad Anwar Panezai, Muhammad Ayub Kakar, et al. "In Vitro Anticancer MCF-7, Anti-Inflammatory, and Brine Shrimp Lethality Assay (BSLA) and GC-MS Analysis of Whole Plant Butanol Fraction of Rheum ribes (WBFRR)." BioMed Research International 2019 (June 23, 2019): 1–8. http://dx.doi.org/10.1155/2019/3264846.

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In this study, GC-MS analysis has shown that whole plant butanol fraction of rheum ribes (WBFRR) comprises of 21 compounds which exhibited anticancer (MCF-7) activity having IC50 value of 36.01± 0.26. MTT assay (MCF-7), Oxidative Burst assay using chemiluminescence technique, and B-Hatching techniques were the methods used for anticancer MCF-7, anti-inflammatory, and Brine Shrimp Lethality Assay (BSLA). GC-MS was used for structural elucidation. Whole plant methanol extract of rheum ribes (WMERR), whole plant n-hexane fraction of rheum ribes (WHFRR), and whole plant aqueous fraction of rheum r
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Misgiati, Misgiati. "POTENSI EKSTRAK N-HEKSAN, DIKLOROMETANA, ETIL ASETAT, DAN ETANOL 70% JAMUR DEWA (Agaricus blazei Murill) TERHADAP SEL MCF-7." Jurnal Riset Kefarmasian Indonesia 4, no. 1 (2022): 11–23. http://dx.doi.org/10.33759/jrki.v4i1.231.

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God mushroom is a functional food. It has pharmacological activity. This content has activity as an anticancer. The purpose of this study was to conduct a preliminary test to obtain an active ingredient capable of having anticancer activity on MCF-7 cells. The stages of the research are stratified extraction with several solvents. Extraction using maceration. The resulting extract was identified and tested for the anticancer activity of MCF-7 cells. The test uses the TLC method. The stationary phase with silica GF254, the mobile phase is n-hexane: ethyl acetate. Anticancer activity test using
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Li, Daichun, Xiaojian Liao, Shenghui Zhong, Bingxin Zhao, and Shihai Xu. "Synthesis of Marine Cyclopeptide Galaxamide Analogues as Potential Anticancer Agents." Marine Drugs 20, no. 3 (2022): 158. http://dx.doi.org/10.3390/md20030158.

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In this paper, eight new galaxamide analogues (Z-1~Z-8) were synthesized and evaluated for their cytotoxic activities against five cancer cell lines, MCF-7, MD-MBA-231, HepG2, Hela, and A549, using MTT assays. The modified analogue Z-6 displayed broad spectrum cytotoxic activity toward each tested cell line with IC50 values of 1.65 ± 0.30 (MCF-7), 2.91 ± 0.17 (HepG2), 4.59 ± 0.27 (MD-MBA-231), 5.69 ± 0.37 (Hela), and 5.96 ± 0.41 (A549) μg/mL, respectively. The galaxamides Z-3 and Z-6 induced concentration-dependent apoptosis of the MCF-7 cells after 72 h as evaluated by the flow cytometry expe
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H Al-Ghamdi, Fuad. "Effect of anticancer electromagnetic spectrums on the cancer cell line growths." Journal of Medical Pharmaceutical and Allied Sciences 13, no. 3 (2024): 6603–7. http://dx.doi.org/10.55522/jmpas.v13i3.6511.

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Electromagnetic frequencies (EMF) that are generated from different electronic devices can interact with biological systems including humans. Several theories described the effects of EMF on the growth of in vitro cancer cell lines and biological systems, which revealed that EMF could inhibit cancer cell growth or decrease viability depending on the field strength and frequency. Accordingly, in this study, we are targeting to assess the effect of the anticancer-extracted electromagnetic spectrums on the growth of two types of cell lines which are the breast cancer cell line MCF-7 and human emb
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Yang, Xiaoting, Zhan Jin, Gao Chen, and Gaobo Hu. "Chloroquine inhibits salinomycin-induced autophagy for collaborative anticancer effect in breast cancer." BioImpacts 15 (May 25, 2025): 30821. https://doi.org/10.34172/bi.30821.

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Introduction: Breast cancer (BC) presents significant morbidity and mortality challenges. Autophagy plays a contradictory role in BC. The chemotherapeutic agent salinomycin exhibits anticancer effects, but its effectiveness is limited by over-activation of autophagy. This study aimed to investigate the effects and mechanisms of salinomycin and its combination with chloroquine in BC. Methods: The MCF-7 and MCF-7 tumor spheroids (MCF-7-TS) BC models were treated separately with salinomycin and autophagy inducer/inhibitor (rapamycin/chloroquine). Cell proliferation, apoptosis, and cell cycle prog
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Gaber, Ahmed, Walaa F. Alsanie, Majid Alhomrani, Abdulhakeem S. Alamri, Ibrahim M. El-Deen, and Moamen S. Refat. "Synthesis of 1-[(Aryl)(3-amino-5-oxopyrazolidin-4-ylidene) methyl]-2-oxo-1,2-dihydroquinoline-3-carboxylic Acid Derivatives and Their Breast Anticancer Activity." Crystals 11, no. 5 (2021): 571. http://dx.doi.org/10.3390/cryst11050571.

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This research aimed to produce new 1-[(aryl)(3-amino-5-oxopyrazolidin-4-ylidene) methyl]-2-oxo-1,2-dihydroquinoline-3-carboxylic acid derivatives and check their anticancer effect against the breast cancer MCF-7 cell line. The 2-oxo-1,2-dihydroquinoline-3-carboxylic acid (4) compound was obtained by hydrolyzing ethyl 2-oxo-1,2-dihydroquinoline-3-carboxylate (2) with thiourea and anhydrous potassium carbonate ethanol, which was then treated with ethyl 3-substituted 2-cyanoacrylates (6) in the presence of triethylamine in diethyl formamide to give 1-[2-(ethoxy)carbonyl-2-cyano-1-arylvinyl]-2-oxo
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Dissertations / Theses on the topic "Anticancer MCF-7"

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Guler, Elif. "Investigaton Of Chemopreventive Properties Ofurtica Dioica L., In Mcf-7 And Mda231 Breast Cancer Celllines." Phd thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613843/index.pdf.

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ABSTRACT INVESTIGATON OF CHEMOPREVENTIVE PROPERTIES OF URTICA DIOICA L., IN MCF-7 AND MDA231 BREAST CANCER CELL LINES. G&uuml<br>ler, Elif Ph.D., Biological Sciences Department Supervisor : Prof. Dr. Mesude
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Zhu, Weiwei. "Effects of Membrane Lateral Organization on the Anticancer Activity of Liposomal CA4P against MCF-7 Breast Cancer Cells." Master's thesis, Temple University Libraries, 2010. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/87353.

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Biochemistry<br>M.S.<br>The goal of this research is to study how the cholesterol content in liposomal formulations affects the anticancer activity (e.g., cell growth suppression) of combretastatin A4 phosphate (CA4P). CA4P is a powerful antivascular agent currently under clinical trials for treating solid tumors. Liposomal CA4P has several advantages over free CA4P, including the reduced toxicities and the increased overall drug efficacy. In this thesis work, I have demonstrated that the proliferation of breast cancer MCF-7 cells varies with the cholesterol mole fraction in the formulation of
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Bai, Zhenlin [Verfasser]. "Substituted Stilbenes and 1,2-Diaryl-1,2-diazidoethanes as Potential Anticancer Agents : Syntheses and Estrogenic / Antiestrogenic Properties in MCF-7-2a Cells / Zhenlin Bai." Berlin : Freie Universität Berlin, 2006. http://d-nb.info/1021818631/34.

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Abrahams, Beynon. "The effects of various combinations of different classes of anticancer drugs and tyrosine kinase inhibitors on the human MCF-7 breast carcinoma cell line." Thesis, University of the Western Cape, 2014. http://hdl.handle.net/11394/3846.

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Magister Scientiae (Medical Bioscience) - MSc(MBS)<br>This study investigated the effects of TKIs on the growth and proliferation of MCF-7 breast carcinoma cells in culture. MCF-7 cells were exposed to different concentrations of TKIs alone and in combination with each other. Inhibition of cell growth by TKIs used individually occurred in a dose- and time-dependent manner. When EGFR Inhibitor I, EGFR Inhibitor II/BIBX1382 and the multi-specific EGFR/ErbB-2/ErB-4 Inhibitor were used in combination with each other at equimolar log dose concentrations, the combined effects on cell growth was sign
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Abrahams, Beynon. "The effects of various combinations of different Cdasses of anticancer drugs and tyrosine kinase inhibitors on the human MCF-7 and triple-negative MDA-MB 231 breast carcinoma cell lines." University of the Western Cape, 2020. http://hdl.handle.net/11394/7881.

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Philosophiae Doctor - PhD<br>Globally, breast cancer is the most common cancer affecting women and it is predicted that in 2030 about 12 million deaths will occur with approximately 21.7 million new cases [2]. Genetic risk factors as well as race and ethnicity, account for about 5-10% of all breast cancer occurrences. Triple negative breast cancer (TNBC), tumors that tested negative for oestrogen receptor (ER), progesterone receptor (PR) and human epidermal growth factor receptor 2 (HER2), contribute to 10-20% of all breast carcinomas [3,4] and is known to be a more aggressive type of cancer w
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Koegle, Eric Richard. "Determining the Intracellular Localization and Efficacy of Novel Anticancer Agents in Human Breast Cancer Cell Lines Through the Use of Fluorescent Microscopy." Connect to full text in OhioLINK ETD Center, 2008. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=toledo1234749487.

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Thesis (M.S.)--University of Toledo, 2008.<br>Typescript. "Submitted as partial fulfillments of the requirements for The Master of Science in Pharmaceutical Sciences in Pharmacology and Toxicology." "A thesis entitled"--at head of title. Bibliography: leaves 47-49.
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Gorincioi, E. "N6-ISOPENTENYL ADENOSINE, A PROMISING ANTICANCER AGENT: SYNTHESIS OF NOVEL ANALOGUES, EVALUATION OF ANTIPROLIFERATIVE ACTIVITY AND INSIGHT INTO ACTION MECHANISM." Doctoral thesis, Università degli Studi di Milano, 2010. http://hdl.handle.net/2434/148874.

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Isopentenyl adenosine (N6-(∆2-Isopentenyl)adenosine, iPAdo) is an important member of the class of cytokinins, N6-substituted adenosines, endowed with hormonal properties in plants. iPAdo is the only known cytokinin existing in animals. Its bioactivity in mammalians has been investigated and the overall reports confirm promising in vitro antiproliferative activity, less pronounced or absent in vivo. The PhD project was initially aimed to investigate this aspect of iPAdo activity and the preparation of iPAdo-grafted gold nanoparticles (GNPs) was selected as a possible solution, due to the well-
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Boshielo, Itumeleng Tania. "In vitro evaluation of anticancer effect on momordica balsamina linn. leaf extract in human MCF-7 cancer cells." Thesis, 2017. http://hdl.handle.net/10386/2487.

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Thesis (M.Sc. (Biochemistry)) --University of Limpopo, 2017<br>Cancer is a broad group of various diseases characterised by unregulated cell proliferation which leads to the formation of tumours (Vickers, 2004). Some tumours remain confined to their site of origin while some gain the ability to spread to other parts of the body, a process known as metastasis (Weiss, 1990). The burden of cancer continues to rise, due to inefficient prevention strategies and serious side effects, as well as the cost of cancer regimens (Sondhi et al., 2010). Medicinal plants represent a reservoir of bioactive com
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Book chapters on the topic "Anticancer MCF-7"

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Suresh, J. Immanuel, and Iswareya Lakshimi V. "Marine Fungal Metabolites." In Handbook of Research on Natural Products and Their Bioactive Compounds as Cancer Therapeutics. IGI Global, 2022. http://dx.doi.org/10.4018/978-1-7998-9258-8.ch010.

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Fungi from marine environments are promising sources of therapeutics against cancer due to the production of various metabolites which contribute against the cancer cell growth and development. Various marine fungal metabolites have been studied against breast and cervical cancer which are the most common causes of death in women. Scopararane I from marine sediment fungi Eutypella sp. FS46 showed better activity against MCF 7. Alterporriol L from marine fungus Alternaria sp. induced cancer cell apoptosis by altering the reactive oxygen species and mitochondrial membrane potential. Apoptosis-in
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Mehra, Vishu, and Isha Lumb. "Recent Synthetic and Biological Advances in Anti-Cancer Ferrocene-Analogues and Hybrids." In Advances in Organic Synthesis. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815040791123180003.

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Cancer is among the most severe risks to the global human population. The enduring crisis of drug-resistant cancer and the limited selectivity of anticancer drugs are significant roadblocks to its control and eradication, requiring the identification of new anticancer entities. The stable aromatic nature, reversible redox properties, and low toxicity of ferrocene revolutionized medicinal organometallic chemistry, providing us with bioferrocene compounds with excellent antiproliferative potential, which has been the focus of persistent efforts in recent years. Substituting the aryl/heteroaryl c
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Hussain, Syed Faisal Jahir, Mohammed Adil A., Durga Munireddy, and Ashok Kumar Kumar Pandurangan. "Effects of Nigella sativa and Its Active Ingredient Thymoquinone on Breast Cancer." In Handbook of Research on Natural Products and Their Bioactive Compounds as Cancer Therapeutics. IGI Global, 2022. http://dx.doi.org/10.4018/978-1-7998-9258-8.ch012.

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Breast cancer (BC) is the most prevalent malignancy in women. The main treatment for BC is surgery and chemotherapy. Generally, the chemotherapeutic drugs used for treatment cause numerous side effects. Substances derived from natural products have proven to exhibit anti-cancer effects without causing side effects. For instance, biochannin A found in cabbage and cauliflower reduced the growth of estrogen dependent MCF 7 cells. Another example is curcumin present in turmeric exhibits anti-proliferative and inhibitory effect against BC. The active compound of Nigella sativa is thymoquinone. The
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Nirmala, Sankaradoss, P. Nadana Sabapathi, and Y. Sravanthi. "Anticancer Activity of Adathoda vasica in Hela, HepG2, MCF-7, MDAMB-231 Cell Lines- In vitro." In Current Overview on Pharmaceutical Science Vol. 2. B P International (a part of SCIENCEDOMAIN International), 2023. http://dx.doi.org/10.9734/bpi/cops/v2/8378f.

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Shajini R, Subitha, Priyaa J. C, Rekha G. S, and Beena Lawrence. "BIOACTIVITY PROFILING OF PUNICA GRANATUM L. FRUIT PARTS." In Futuristic Trends in Biotechnology Volume 3 Book 3. Iterative International Publisher, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bfbt3p1ch6.

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Punica granatum L. is a traditional medicinal plant highly acclaimed for its fruit. The fruit is used as a remedy to boost immunity during sickness. The fruits are rich in many secondary metabolites of prime importance like flavonoids, alkaloids, polyphenols, tannins etc. In the present investigation an attempt was made to profile the biological efficacy of the peel and pulp of the fruit through phytochemistry, GCMS analysis, anticancer screening and in silico analysis. Phytochemical profiling of ethanolic extract of peel and pulp of fruits showed the presence of more amounts of flavonoids, ta
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"From nature to nuclear application: The anticancer potential of radiolabeled Pinus pinea extract." In Book of Abstracts - RAD 2025 Conference. RAD Centre, Niš, Serbia, 2025. https://doi.org/10.21175/rad.abstr.book.2025.26.3.

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Breast cancer is the most commonly diagnosed cancer among women and holds a significant place among cancer-related mortalities worldwide. Ovarian cancer, on the other hand, is often diagnosed at an advanced stage and is known to have the highest mortality rate among gynecological malignancies. Traditional cancer treatment methods, including surgery, chemotherapy, and radiotherapy, are widely used; however, these approaches are associated with high costs and can also cause severe side effects by damaging healthy cells. This has increased the need for more targeted therapeutic strategies with re
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Vimala J, Rosaline, Stella Bharathy, M. Agila A, Margret Sheela S, and Vimala S. "PHYTO SYNTHESIS OF ZINC OXIDE NANOPARTICLES MEDIATED BY FLAVONOID FRACTION EXTRACTED FROM MELIA DUBIA BARK AND ITS ANTIOXIDANT, ANTICANCER AND PHOTOCATALYTIC ACTIVITY." In Futuristic Trends in Chemical Material Sciences & Nano Technology Volume 3 Book 16. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bjcs16p2ch2.

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Numerous Phytochemicals have been successfully tested for their strong biological activity, and the results have been positive. For the "green" synthesis of metal nanoparticles, flavonoids found in plant materials function as reducing and electrostatic stabilising agents. In addition, these nanomaterials are useful for treating different cancer cells as well as harmful microbes. Hence, in the present research work flavonoids was used in the preparation of zinc oxide nanoparticles. Flavonoids’ decreased bioavailability due to its poorer solubility in aqueous medium limits the use of such dietar
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Citi, Valentina, Alma Martelli, Eugenia Piragine, et al. "Anticancer Effect of a Novel H2S-Hybrid Molecule on Human Breast Adenocarcinoma (MFC-7) and Human Breast Epithelial (MCF-10A) Cell Lines." In Therapeutic Application of Nitric Oxide in Cancer and Inflammatory Disorders. Elsevier, 2019. http://dx.doi.org/10.1016/b978-0-12-816545-4.00019-0.

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Yılmaz, Bahar. "Investigation of the Death Effects of Four Different Chemotherapeutic Agents on Breast Cancer Cell Lines under the Microscope." In Versatile Approaches to Engineering and Applied Sciences: Materials and Methods. Özgür Yayınları, 2023. http://dx.doi.org/10.58830/ozgur.pub50.c71.

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Cancer is usually called continuous and fast growing tumor cells. It is a disease characterized by uncontrolled growth and metastasis by activation of oncogenes, epigenetic modifications, inactivation of tumor suppressors. Treatments are based on researched methods with the aim of minimizing tumor progression, recurrence and mortality. Generally, many treatment methods are applied, especially chemotherapy, radiotherapy and surgical methods. Cytotoxic chemotherapy is most commonly used. Since these chemotherapies target all body cells, they can damage some healthy cells as well as cancer cells.
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Arul Priya, R., K. Saravanan, and B. Umarani. "Gas chromatography-mass spectrometry analysis and in vitro anticancer activity of tectona grandis bark extract against human breast cancer cell line (mcf-7)." In Phytochemistry. Apple Academic Press, 2018. http://dx.doi.org/10.1201/9780429426223-23.

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Conference papers on the topic "Anticancer MCF-7"

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Salehi, H., E. Middendorp, A.-G. Végh, S.-K. Ramakrishnan, C. Gergely, and F. J. G. Cuisinier. "Detection of apoptosis caused by anticancer drug paclitaxel in MCF-7 cells by confocal Raman microscopy." In SPIE BiOS, edited by Alexander N. Cartwright and Dan V. Nicolau. SPIE, 2013. http://dx.doi.org/10.1117/12.1000149.

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Radomska, Dominika, Dominik Radomski, Robert Czarnomysy, and Krzysztof Bielawski. "Anticancer activity of novel selenoesters in MCF-7 and MDA-MB-231 human breast cancer cells." In RAD Conference. RAD Centre, 2021. http://dx.doi.org/10.21175/rad.abstr.book.2021.8.5.

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Pasaribu, Gunawan, and Totok Waluyo. "Anticancer activity of Saurauia vulcani extract in various solvents on HeLa and MCF-7 cell line." In THE 2ND INTERNATIONAL CONFERENCE OF LIGNOCELLULOSE. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0184564.

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Senthilkumaran, C. K., and S. Sugapriya. "Anticancer Activity of Silver Nan Particles against Cell Line MCF-7–Human - Breast Cancer through MTT Assay." In Proceedings of the First International Conference on Combinatorial and Optimization, ICCAP 2021, December 7-8 2021, Chennai, India. EAI, 2021. http://dx.doi.org/10.4108/eai.7-12-2021.2314712.

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Adiyoga, Reza, Irma Isnafia Arief, and Cahyo Budiman. "Anticancer Potential of Lactobacillus acidophilus IIA-2B4 Extracts Against MCF-7 Breast Cancer Cell Line." In 9th International Seminar on Tropical Animal Production (ISTAP 2021). Atlantis Press, 2022. http://dx.doi.org/10.2991/absr.k.220207.041.

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Riswandi, Riswandi, Prihantono Prihantono, Indah Raya, and Rizal Irfandi. "Potential of Breast Anticancer Compounds (MCF-7) from Synthesis Results and Characterization of Complex Compounds of Mg(II) Isoleucinedithiocarbamate." In 1st International Conference on Science and Technology, ICOST 2019, 2-3 May, Makassar, Indonesia. EAI, 2019. http://dx.doi.org/10.4108/eai.2-5-2019.2284630.

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Ganur, Alicia N. A., Dyah U. C. Rahayu, Hanhan Dianhar, Ichsan Irwanto, and Purwantiningsih Sugita. "Terpenoid from Indonesian temu mangga (Curcuma mangga, Val) rhizomes and review of its anticancer towards MCF-7 breast cells." In 4TH INTERNATIONAL SEMINAR ON CHEMISTRY. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0051538.

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"Biogenic Zinc Oxide Nanoparticles Synthesis Using Tabernaemontana Divaricate Leaf Extract and Its Anticancer Activity against MCF-7 Breast Cancer Cell Lines." In International Conference on Advances in Agricultural, Biological & Environmental Sciences. International Institute of Chemical, Biological & Environmental Engineering, 2014. http://dx.doi.org/10.15242/iicbe.c1014032.

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Sianipar, Nesti Fronika, Khoirunnisa Assidqi, Yuni Elsa Hadisaputri, Ragapadmi Purnamaningsih, and Idris Gautama So. "Anticancer activity and MRNA expression of rodent tuber mutant (Typhonium flagelliforme) extract against breast cancer cell line MCF-7 in vitro." In 2ND INTERNATIONAL CONFERENCE ON INDUSTRY-ACADEMIA INITIATIVES IN BIOTECHNOLOGY AND CHEMISTRY (iCIABC2023). AIP Publishing, 2025. https://doi.org/10.1063/5.0249430.

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Levovnik, Bojan D., Aleksa P. Alargić, Miloš M. Svirčev, and Goran I. Benedeković. "Building a 3D QSAR model with isopropylidene analogs of cytotoxic styryl-lactones." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.559l.

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Styryl-lactones are a class of natural products and related analogs that exhibit diverse biological activities, including anticancer, anti-inflammatory, and antimicrobial properties. Since these compounds are routinely obtained in our laboratory from their O-isopropylidene precursors, we envisioned the project to examine and compare their respective structures and in-vitro activities. This paper presents a basic 3D-QSAR steric model built on a small set of 11 selected O-isopropylidene and styryl-lactone (particularly [3.3.0]furofuranone) ligands and their in vitro activities against an MCF-7 c
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You might also be interested in the extended bibliographies on the topic 'Anticancer MCF-7' for particular source types:
Journal articles
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