Page last updated: 2024-10-17

lactic acid and Cell Transformation, Neoplastic

lactic acid has been researched along with Cell Transformation, Neoplastic in 74 studies

Lactic Acid: A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
2-hydroxypropanoic acid : A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.

Cell Transformation, Neoplastic: Cell changes manifested by escape from control mechanisms, increased growth potential, alterations in the cell surface, karyotypic abnormalities, morphological and biochemical deviations from the norm, and other attributes conferring the ability to invade, metastasize, and kill.

Research Excerpts

ExcerptRelevanceReference
"The nutrient demands of cancer cannot be met by normal cell metabolism."2.52Sirtuins and the Metabolic Hurdles in Cancer. ( German, NJ; Haigis, MC, 2015)
"MCT4 and Cav-1 are also breast cancer prognostic biomarkers."2.50Tumor microenvironment and metabolic synergy in breast cancers: critical importance of mitochondrial fuels and function. ( Lisanti, MP; Martinez-Outschoorn, U; Sotgia, F, 2014)
" Their efficacy has been tested in tumor xenografted mice and considerable experimental findings have stimulated researchers to further improve the bioavailability of these nutraceuticals."2.50Targeting cancer with nano-bullets: curcumin, EGCG, resveratrol and quercetin on flying carpets. ( Aras, A; Farooqi, AA; Hechenleitner, AA; Khokhar, AR; Pineda, EA; Qureshi, MZ; Silva, MF; Sobczak-Kupiec, A, 2014)
"Given its pleiotropic effects on cancer biology, PKM2 represents an attractive target for cancer therapy."2.48Emerging roles of PKM2 in cell metabolism and cancer progression. ( Luo, W; Semenza, GL, 2012)
"Low lactate tumors (8 micromol/g)."2.42Lactate: mirror and motor of tumor malignancy. ( Mueller-Klieser, WF; Walenta, S, 2004)
"Lactic acidosis is a feature of solid tumors and plays fundamental role(s) rendering cancer cells to adapt to diverse metabolic stresses, but the mechanism underlying its roles in redox homeostasis remains elusive."1.91A GSTP1-mediated lactic acid signaling promotes tumorigenesis through the PPP oxidative branch. ( Ahmad, M; Chen, C; He, Q; Hu, Y; Li, J; Lin, Y; Luo, H; Luo, Y; Sun, Y; Wang, B; Wu, D; Yang, Z; Zheng, L, 2023)
"Individuals with hepatocellular carcinoma who responded to anti-PD-1 treatment have lower levels of MOESIN lactylation in Treg cells than nonresponding individuals."1.72Tumor metabolite lactate promotes tumorigenesis by modulating MOESIN lactylation and enhancing TGF-β signaling in regulatory T cells. ( Chen, Q; Gao, J; Gu, J; Li, X; Liang, Y; Lu, L; Shao, Q; Wang, Q; Wei, S; Xu, X; Zhou, B; Zhou, H; Zhou, J, 2022)
"SLC1A3 was found to be overexpressed in gastric cancer, and this overexpression was associated with poor prognosis."1.56SLC1A3 promotes gastric cancer progression via the PI3K/AKT signalling pathway. ( Awaleh Moumin, F; Cai, J; Chen, J; Chen, X; Jia, L; Xu, L, 2020)
"Malignant tumors, such as colorectal cancer (CRC), are heterogeneous diseases characterized by distinct metabolic phenotypes."1.48Nuclear factor E2-related factor-2 has a differential impact on MCT1 and MCT4 lactate carrier expression in colonic epithelial cells: a condition favoring metabolic symbiosis between colorectal cancer and stromal cells. ( Ammar, N; Arlt, A; Diehl, K; Dinges, LA; Helm, O; Plundrich, D; Röcken, C; Schäfer, H; Sebens, S, 2018)
"Three ovarian cancer cell lines, HEY, SKOV3, and IGROV-1, were assayed for glutamine dependence by analyzing cytotoxicity, cell cycle progression, apoptosis, cell stress, and glucose/glutamine metabolism."1.42Glutamine promotes ovarian cancer cell proliferation through the mTOR/S6 pathway. ( Bae-Jump, VL; Guo, H; Jones, HM; Roque, DR; Sheng, X; Stine, JE; Willson, AK; Yuan, L; Zhou, C, 2015)
"An altered metabolism during ovarian cancer progression allows for increased macromolecular synthesis and unrestrained growth."1.40Ovarian tumor-initiating cells display a flexible metabolism. ( Anderson, AS; Frisard, MI; Hulver, MW; Roberts, PC; Schmelz, EM, 2014)
"Withaferin A (WA) is a bioactive compound derived from Withania somnifera."1.39Withaferin A suppresses tumor promoter 12-O-tetradecanoylphorbol 13-acetate-induced decreases in isocitrate dehydrogenase 1 activity and mitochondrial function in skin epidermal JB6 cells. ( Li, W; Zhao, Y, 2013)
"Recent studies have suggested that cancer cells behave as metabolic parasites, by inducing oxidative stress in adjacent normal fibroblasts."1.38Mitochondrial fission induces glycolytic reprogramming in cancer-associated myofibroblasts, driving stromal lactate production, and early tumor growth. ( Ando', S; Aquila, S; Casimiro, MC; Guido, C; Howell, A; Lin, Z; Lisanti, MP; Martinez-Outschoorn, UE; Pestell, RG; Sotgia, F; Whitaker-Menezes, D; Zimmers, TA, 2012)
"Its promoter was hypermethylated in gastric cancer cell lines (57%, 4/7) and gastric carcinomas (33%, 33/101)."1.36Warburg effect revisited: an epigenetic link between glycolysis and gastric carcinogenesis. ( Chan, FK; Cheng, AS; Jin, HC; Lam, EK; Liu, X; Shin, VY; Sung, JJ; Wang, X; Yu, J; Zhang, J, 2010)
"Necrosis was present histologically in four of the five meningiomas classified either as atypical or papillary."1.30Noninvasive evaluation of the malignant potential of intracranial meningiomas performed using proton magnetic resonance spectroscopy. ( Handa, J; Inubushi, T; Matsuda, M; Morikawa, S; Nakasu, S; Shino, A, 1999)

Research

Studies (74)

TimeframeStudies, this research(%)All Research%
pre-19905 (6.76)18.7374
1990's6 (8.11)18.2507
2000's12 (16.22)29.6817
2010's38 (51.35)24.3611
2020's13 (17.57)2.80

Authors

AuthorsStudies
Man, CH1
Mercier, FE1
Liu, N1
Dong, W1
Stephanopoulos, G1
Jiang, L1
Jung, Y1
Lin, CP1
Leung, AYH1
Scadden, DT1
Pan, L1
Feng, F1
Wu, J3
Fan, S1
Han, J1
Wang, S1
Yang, L2
Liu, W1
Wang, C2
Xu, K1
Gu, J1
Zhou, J1
Chen, Q1
Xu, X1
Gao, J1
Li, X2
Shao, Q1
Zhou, B1
Zhou, H1
Wei, S1
Wang, Q1
Liang, Y1
Lu, L1
Gao, X1
Zhou, S1
Qin, Z1
Li, D1
Zhu, Y1
Ma, D1
Sun, Q1
Zhu, G1
Li, T1
Zhu, X1
Ni, B1
Xu, B1
Ma, X2
Li, J4
Wang, T1
Ye, Z1
Li, Z2
Jing, DS1
Fan, GX1
Liu, MQ1
Zhuo, QF1
Ji, SR1
Yu, XJ1
Xu, XW1
Qin, Y1
Sun, Y1
He, Q1
Yang, Z1
Ahmad, M1
Lin, Y1
Wu, D1
Zheng, L1
Wang, B1
Chen, C1
Hu, Y1
Luo, H1
Luo, Y1
Bhagat, TD1
Von Ahrens, D1
Dawlaty, M1
Zou, Y2
Baddour, J1
Achreja, A1
Zhao, H1
Patel, B1
Kwak, C1
Choudhary, GS1
Gordon-Mitchell, S1
Aluri, S1
Bhattacharyya, S1
Sahu, S1
Bhagat, P1
Yu, Y1
Bartenstein, M1
Giricz, O1
Suzuki, M1
Sohal, D1
Gupta, S1
Guerrero, PA1
Batra, S1
Goggins, M1
Steidl, U1
Greally, J1
Agarwal, B1
Pradhan, K1
Banerjee, D1
Nagrath, D1
Maitra, A1
Verma, A1
Sheng, Y1
Jiang, Q1
Dong, X1
Liu, J1
Liu, L1
Wang, H1
Wang, L2
Li, H2
Yang, X1
Dong, J1
Yuan, Y1
Sun, L1
Wang, X3
Chen, J3
Jia, M1
Sa, H1
Cai, Y1
Xu, Y1
Sun, C1
Guo, Y2
Ma, K1
Gándara, L1
Durrieu, L1
Behrensen, C1
Wappner, P1
Mendes, C1
Serpa, J1
Lee, S1
Jo, G1
Jung, JS1
Yang, DH1
Hyun, H1
Xu, L1
Jia, L1
Chen, X3
Awaleh Moumin, F1
Cai, J1
Broadfield, LA1
Duarte, JAG1
Schmieder, R1
Broekaert, D1
Veys, K1
Planque, M1
Vriens, K1
Karasawa, Y1
Napolitano, F1
Fujita, S1
Fujii, M1
Eto, M1
Holvoet, B1
Vangoitsenhoven, R1
Fernandez-Garcia, J1
Van Elsen, J1
Dehairs, J1
Zeng, J1
Dooley, J1
Rubio, RA1
van Pelt, J1
Grünewald, TGP1
Liston, A1
Mathieu, C1
Deroose, CM1
Swinnen, JV1
Lambrechts, D1
di Bernardo, D1
Kuroda, S1
De Bock, K1
Fendt, SM1
Zhou, C2
Li, L1
Wang, Y2
Xing, Y1
Fu, J1
Yao, B1
Chang, B1
Zhao, P1
Kon, S1
Ishibashi, K1
Katoh, H1
Kitamoto, S1
Shirai, T1
Tanaka, S1
Kajita, M1
Ishikawa, S1
Yamauchi, H1
Yako, Y1
Kamasaki, T1
Matsumoto, T1
Watanabe, H1
Egami, R1
Sasaki, A1
Nishikawa, A1
Kameda, I1
Maruyama, T1
Narumi, R1
Morita, T1
Sasaki, Y1
Enoki, R1
Honma, S1
Imamura, H1
Oshima, M1
Soga, T1
Miyazaki, JI1
Duchen, MR1
Nam, JM1
Onodera, Y1
Yoshioka, S1
Kikuta, J1
Ishii, M1
Imajo, M1
Nishida, E1
Fujioka, Y1
Ohba, Y1
Sato, T1
Fujita, Y1
Diehl, K1
Dinges, LA1
Helm, O1
Ammar, N1
Plundrich, D1
Arlt, A1
Röcken, C1
Sebens, S1
Schäfer, H1
Chen, H1
Gao, S1
Cheng, C1
Apicella, M1
Giannoni, E1
Fiore, S1
Ferrari, KJ1
Fernández-Pérez, D1
Isella, C1
Granchi, C1
Minutolo, F1
Sottile, A1
Comoglio, PM1
Medico, E1
Pietrantonio, F1
Volante, M1
Pasini, D1
Chiarugi, P1
Giordano, S1
Corso, S1
Feng, R1
Morine, Y1
Ikemoto, T1
Imura, S1
Iwahashi, S1
Saito, Y1
Shimada, M1
Updegraff, BL1
Zhou, X1
Padanad, MS1
Chen, PH1
Yang, C2
Sudderth, J1
Rodriguez-Tirado, C1
Girard, L1
Minna, JD1
Mishra, P1
DeBerardinis, RJ1
O'Donnell, KA1
Rai, A1
Greening, DW1
Chen, M1
Xu, R1
Ji, H1
Simpson, RJ1
Schwörer, S1
Vardhana, SA1
Thompson, CB1
Zheng, W1
Tayyari, F1
Gowda, GA1
Raftery, D1
McLamore, ES1
Porterfield, DM1
Donkin, SS1
Bequette, B1
Teegarden, D1
Hipp, NI1
Christner, L1
Wirth, T1
Mueller-Klieser, W2
Walenta, S2
Schröck, E1
Debatin, KM1
Beltinger, C1
Doherty, JR1
Scott, KE1
Cameron, MD1
Fallahi, M1
Li, W2
Hall, MA1
Amelio, AL1
Mishra, JK1
Li, F1
Tortosa, M1
Genau, HM1
Rounbehler, RJ1
Lu, Y2
Dang, CV1
Kumar, KG1
Butler, AA1
Bannister, TD1
Hooper, AT1
Unsal-Kacmaz, K1
Roush, WR1
Cleveland, JL1
Li, G1
Mao, F1
Liu, Q1
Chen, L1
Lv, L1
Dai, W1
Wang, G1
Zhao, E1
Tang, KF1
Sun, ZS1
Martinez-Outschoorn, U2
Sotgia, F3
Lisanti, MP3
Aras, A1
Khokhar, AR1
Qureshi, MZ1
Silva, MF1
Sobczak-Kupiec, A1
Pineda, EA1
Hechenleitner, AA1
Farooqi, AA1
Bi, P1
Burcham, G1
Elzey, BD1
Ratliff, T1
Konieczny, SF1
Ahmad, N1
Kuang, S1
Liu, X2
Anderson, AS1
Roberts, PC1
Frisard, MI1
Hulver, MW1
Schmelz, EM1
Campbell, DF1
Saenz, R1
Bharati, IS1
Seible, D1
Zhang, L2
Esener, S1
Messmer, B1
Larsson, M1
Messmer, D1
Yuan, L1
Sheng, X1
Willson, AK1
Roque, DR1
Stine, JE1
Guo, H1
Jones, HM1
Bae-Jump, VL1
Peng, C1
Su, J1
Zeng, W1
Zhang, X1
German, NJ1
Haigis, MC1
Walker, CM1
Chen, Y1
Lai, SY1
Bankson, JA1
Peruzzo, P1
Comelli, M1
Di Giorgio, E1
Franforte, E1
Mavelli, I1
Brancolini, C1
Calamita, P1
Miluzio, A1
Russo, A1
Pesce, E1
Ricciardi, S1
Khanim, F1
Cheroni, C1
Alfieri, R1
Mancino, M1
Gorrini, C1
Rossetti, G1
Peluso, I1
Pagani, M1
Medina, DL1
Rommens, J1
Biffo, S1
Frank, H1
Gröger, N1
Diener, M1
Becker, C1
Braun, T1
Boettger, T1
Backshall, A1
Alferez, D1
Teichert, F1
Wilson, ID1
Wilkinson, RW1
Goodlad, RA1
Keun, HC2
de Groof, AJ1
te Lindert, MM1
van Dommelen, MM1
Wu, M1
Willemse, M1
Smift, AL1
Winer, M1
Oerlemans, F1
Pluk, H1
Fransen, JA1
Wieringa, B1
Zhang, J2
Lam, EK1
Shin, VY1
Cheng, AS1
Yu, J1
Chan, FK1
Sung, JJ1
Jin, HC1
Cho, HS1
Dong, Z1
Pauletti, GM1
Xu, H1
Gu, H1
Ewing, RC1
Huth, C1
Wang, F1
Shi, D1
Le Floch, R1
Chiche, J1
Marchiq, I1
Naiken, T2
Ilc, K1
Ilk, K1
Murray, CM1
Critchlow, SE1
Roux, D1
Simon, MP1
Pouysségur, J1
Yuneva, MO1
Fan, TW1
Allen, TD1
Higashi, RM1
Ferraris, DV1
Tsukamoto, T1
Matés, JM1
Alonso, FJ1
Seo, Y1
Bishop, JM1
Luo, W1
Semenza, GL1
Guido, C2
Whitaker-Menezes, D2
Capparelli, C1
Balliet, R1
Lin, Z2
Pestell, RG2
Howell, A2
Aquila, S2
Andò, S1
Zimmers, TA1
Casimiro, MC1
Ando', S1
Martinez-Outschoorn, UE1
Locasale, JW1
Zhao, Y1
Yang, W1
Xia, Y1
Cao, Y1
Zheng, Y1
Bu, W1
You, MJ1
Koh, MY1
Cote, G1
Aldape, K1
Li, Y1
Verma, IM1
Chiao, PJ1
Lu, Z1
Jiménez, B1
Mirnezami, R1
Kinross, J1
Cloarec, O1
Holmes, E1
Goldin, RD1
Ziprin, P1
Darzi, A1
Nicholson, JK1
Huber, AL1
Lebeau, J1
Guillaumot, P1
Pétrilli, V1
Malek, M1
Chilloux, J1
Fauvet, F1
Payen, L1
Kfoury, A1
Renno, T1
Chevet, E1
Manié, SN1
Salnikow, K1
Davidson, T1
Costa, M1
Mueller-Klieser, WF1
Chiaradonna, F1
Sacco, E1
Manzoni, R1
Giorgio, M1
Vanoni, M1
Alberghina, L1
Fantin, VR1
St-Pierre, J1
Leder, P1
Funes, JM1
Quintero, M1
Henderson, S1
Martinez, D1
Qureshi, U1
Westwood, C1
Clements, MO1
Bourboulia, D1
Pedley, RB1
Moncada, S1
Boshoff, C1
Huang, KH1
Liu, JH1
Zhu, ZH1
Li, XX1
Lu, XP1
Zhou, SY1
Kawauchi, K1
Araki, K1
Tobiume, K1
Tanaka, N1
Peterkofsky, B1
Kalwinsky, D1
Chauhan, U1
Prather, W1
Assad, R1
Sens, DA1
Hochstadt, B1
Amos, H1
Mothersill, C1
Seymour, CB1
Moriarty, M1
Kaplan, AE1
Yamaguchi, MK1
Tralka, TS1
Hanna, CH1
Anghileri, LJ1
Maincent, P1
Thouvenot, P1
Cordova-Martinez, A1
Nyberg, SL1
Remmel, RP1
Mann, HJ1
Peshwa, MV1
Hu, WS1
Cerra, FB1
Tedeschi, G1
Lundbom, N1
Raman, R1
Bonavita, S1
Duyn, JH1
Alger, JR1
Di Chiro, G1
Shino, A1
Nakasu, S1
Matsuda, M1
Handa, J1
Morikawa, S1
Inubushi, T1
Kunz-Schughart, LA1
Doetsch, J1
Groebe, K1
Wu, H1
Scher, BM1
Chu, CL1
Leonard, M1
Olmedo, R1
Scher, GS1
Stecker, S1
Scher, W1
Waxman, S1
Andersen, JK1
Zhang, MB1
Zhong, XH1
Rozenberg, YY1
Howard, BD1
Jullien, P1
Berg, TM1
Lawrence, DA1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
18F-FDG Metabolism Imaging Monitoring Non-small Cell Lung Cancer Curative Effect of Chemotherapy Multicenter Clinical Study[NCT02938546]Phase 3200 participants (Anticipated)Interventional2016-11-30Not yet recruiting
What Are the Factors Affecting Neoadjuvant Chemotherapy Efficacy in Breast Cancer? A Non-invasive in Vivo Study Using Specialist Magnetic Resonance (MR) Methods[NCT03501394]25 participants (Anticipated)Interventional2018-05-02Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

9 reviews available for lactic acid and Cell Transformation, Neoplastic

ArticleYear
Lactate-related metabolic reprogramming and immune regulation in colorectal cancer.
    Frontiers in endocrinology, 2022, Volume: 13

    Topics: Carcinogenesis; Cell Transformation, Neoplastic; Colorectal Neoplasms; Glycolysis; Humans; Lactic Ac

2022
Lactate-induced protein lactylation: A bridge between epigenetics and metabolic reprogramming in cancer.
    Cell proliferation, 2023, Volume: 56, Issue:10

    Topics: Carcinogenesis; Cell Transformation, Neoplastic; Epigenesis, Genetic; Histones; Humans; Lactic Acid;

2023
Revisiting lactate dynamics in cancer-a metabolic expertise or an alternative attempt to survive?
    Journal of molecular medicine (Berlin, Germany), 2020, Volume: 98, Issue:10

    Topics: Animals; Cell Survival; Cell Transformation, Neoplastic; Energy Metabolism; Glycolysis; Humans; Lact

2020
Cancer Metabolism Drives a Stromal Regenerative Response.
    Cell metabolism, 2019, 03-05, Volume: 29, Issue:3

    Topics: Amino Acids; Animals; Carcinogenesis; Cell Line, Tumor; Cell Transformation, Neoplastic; Glucose; Hu

2019
Tumor microenvironment and metabolic synergy in breast cancers: critical importance of mitochondrial fuels and function.
    Seminars in oncology, 2014, Volume: 41, Issue:2

    Topics: Animals; Autophagy; Breast Neoplasms; Cachexia; Carcinoma; Caveolin 1; Cell Line, Tumor; Cell Transf

2014
Targeting cancer with nano-bullets: curcumin, EGCG, resveratrol and quercetin on flying carpets.
    Asian Pacific journal of cancer prevention : APJCP, 2014, Volume: 15, Issue:9

    Topics: Animals; Anticarcinogenic Agents; Antineoplastic Agents; Antioxidants; Apoptosis; Catechin; Cell Pro

2014
Sirtuins and the Metabolic Hurdles in Cancer.
    Current biology : CB, 2015, Jun-29, Volume: 25, Issue:13

    Topics: Biosynthetic Pathways; Cell Transformation, Neoplastic; Energy Metabolism; Gluconeogenesis; Humans;

2015
Emerging roles of PKM2 in cell metabolism and cancer progression.
    Trends in endocrinology and metabolism: TEM, 2012, Volume: 23, Issue:11

    Topics: Animals; Carrier Proteins; Cell Proliferation; Cell Transformation, Neoplastic; Disease Progression;

2012
Lactate: mirror and motor of tumor malignancy.
    Seminars in radiation oncology, 2004, Volume: 14, Issue:3

    Topics: Cell Hypoxia; Cell Transformation, Neoplastic; Female; Humans; Hyaluronic Acid; Hypoxia-Inducible Fa

2004

Other Studies

65 other studies available for lactic acid and Cell Transformation, Neoplastic

ArticleYear
Proton export alkalinizes intracellular pH and reprograms carbon metabolism to drive normal and malignant cell growth.
    Blood, 2022, 01-27, Volume: 139, Issue:4

    Topics: Animals; Carbon; Cell Proliferation; Cell Transformation, Neoplastic; Humans; Hydrogen-Ion Concentra

2022
Demethylzeylasteral targets lactate by inhibiting histone lactylation to suppress the tumorigenicity of liver cancer stem cells.
    Pharmacological research, 2022, Volume: 181

    Topics: Animals; Carcinogenesis; Carcinoma, Hepatocellular; Cell Line, Tumor; Cell Proliferation; Cell Trans

2022
Tumor metabolite lactate promotes tumorigenesis by modulating MOESIN lactylation and enhancing TGF-β signaling in regulatory T cells.
    Cell reports, 2022, 06-21, Volume: 39, Issue:12

    Topics: Animals; Carcinoma, Hepatocellular; Cell Transformation, Neoplastic; Lactic Acid; Liver Neoplasms; M

2022
Upregulation of HMGB1 in tumor-associated macrophages induced by tumor cell-derived lactate further promotes colorectal cancer progression.
    Journal of translational medicine, 2023, 01-28, Volume: 21, Issue:1

    Topics: Animals; Carcinogenesis; Cell Line, Tumor; Cell Movement; Cell Transformation, Neoplastic; Colorecta

2023
A GSTP1-mediated lactic acid signaling promotes tumorigenesis through the PPP oxidative branch.
    Cell death & disease, 2023, 07-25, Volume: 14, Issue:7

    Topics: Carcinogenesis; Cell Transformation, Neoplastic; Glucosephosphate Dehydrogenase; Glutathione S-Trans

2023
Lactate-mediated epigenetic reprogramming regulates formation of human pancreatic cancer-associated fibroblasts.
    eLife, 2019, 11-01, Volume: 8

    Topics: 5-Methylcytosine; Animals; Cancer-Associated Fibroblasts; Carcinoma, Pancreatic Ductal; Cell Line, T

2019
3-Bromopyruvate inhibits the malignant phenotype of malignantly transformed macrophages and dendritic cells induced by glioma stem cells in the glioma microenvironment via miR-449a/MCT1.
    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2020, Volume: 121

    Topics: Cell Transformation, Neoplastic; Cells, Cultured; Dendritic Cells; Glioma; Lactic Acid; Macrophages;

2020
Identification of a new
    Future oncology (London, England), 2019, Volume: 15, Issue:36

    Topics: Alternative Splicing; Animals; Base Sequence; Cell Cycle Proteins; Cell Line, Tumor; Cell Proliferat

2019
A genetic toolkit for the analysis of metabolic changes in Drosophila provides new insights into metabolic responses to stress and malignant transformation.
    Scientific reports, 2019, 12-27, Volume: 9, Issue:1

    Topics: Animals; Cell Line, Tumor; Cell Proliferation; Cell Transformation, Neoplastic; Drosophila melanogas

2019
Near-infra-red fluorescent chitosan oligosaccharide lactate for targeted cancer imaging and photothermal therapy.
    Artificial cells, nanomedicine, and biotechnology, 2020, Volume: 48, Issue:1

    Topics: Animals; Cell Line, Tumor; Cell Transformation, Neoplastic; Chitosan; Fluorescent Dyes; Humans; Infr

2020
SLC1A3 promotes gastric cancer progression via the PI3K/AKT signalling pathway.
    Journal of cellular and molecular medicine, 2020, Volume: 24, Issue:24

    Topics: Adenosine Triphosphate; Animals; Apoptosis; Biomarkers; Cell Line, Tumor; Cell Survival; Cell Transf

2020
Fat Induces Glucose Metabolism in Nontransformed Liver Cells and Promotes Liver Tumorigenesis.
    Cancer research, 2021, 04-15, Volume: 81, Issue:8

    Topics: Animals; Carcinoma, Hepatocellular; Cell Transformation, Neoplastic; Citric Acid Cycle; Diet, High-F

2021
Untargeted metabolomics and lipidomics analysis identified the role of FOXA1 in remodeling the metabolic pattern of BaP-transformed 16HBE cells.
    Toxicology and applied pharmacology, 2021, 09-01, Volume: 426

    Topics: Adenosine Triphosphate; Benzo(a)pyrene; Carcinogens; Cell Line; Cell Transformation, Neoplastic; Cit

2021
Cell competition with normal epithelial cells promotes apical extrusion of transformed cells through metabolic changes.
    Nature cell biology, 2017, Volume: 19, Issue:5

    Topics: Animals; Cell Communication; Cell Line, Transformed; Cell Transformation, Neoplastic; Coculture Tech

2017
Nuclear factor E2-related factor-2 has a differential impact on MCT1 and MCT4 lactate carrier expression in colonic epithelial cells: a condition favoring metabolic symbiosis between colorectal cancer and stromal cells.
    Oncogene, 2018, 01-04, Volume: 37, Issue:1

    Topics: Apoptosis; Biopsy; Cell Line, Tumor; Cell Transformation, Neoplastic; Coculture Techniques; Colon; C

2018
MiR-323a-3p suppressed the glycolysis of osteosarcoma via targeting LDHA.
    Human cell, 2018, Volume: 31, Issue:4

    Topics: Cell Line; Cell Line, Tumor; Cell Transformation, Neoplastic; Gene Expression; Gene Targeting; Glyco

2018
Increased Lactate Secretion by Cancer Cells Sustains Non-cell-autonomous Adaptive Resistance to MET and EGFR Targeted Therapies.
    Cell metabolism, 2018, 12-04, Volume: 28, Issue:6

    Topics: Animals; Antineoplastic Agents; Cancer-Associated Fibroblasts; Cell Line, Tumor; Cell Transformation

2018
Nrf2 activation drive macrophages polarization and cancer cell epithelial-mesenchymal transition during interaction.
    Cell communication and signaling : CCS, 2018, 09-04, Volume: 16, Issue:1

    Topics: Cell Communication; Cell Movement; Cell Transformation, Neoplastic; Epithelial-Mesenchymal Transitio

2018
Transmembrane Protease TMPRSS11B Promotes Lung Cancer Growth by Enhancing Lactate Export and Glycolytic Metabolism.
    Cell reports, 2018, 11-20, Volume: 25, Issue:8

    Topics: Basigin; Biological Transport; Carcinogenesis; Cell Line, Tumor; Cell Membrane; Cell Proliferation;

2018
Exosomes Derived from Human Primary and Metastatic Colorectal Cancer Cells Contribute to Functional Heterogeneity of Activated Fibroblasts by Reprogramming Their Proteome.
    Proteomics, 2019, Volume: 19, Issue:8

    Topics: Amino Acid Transport System ASC; Cell Proliferation; Cell Transformation, Neoplastic; Colonic Neopla

2019
Altered glucose metabolism in Harvey-ras transformed MCF10A cells.
    Molecular carcinogenesis, 2015, Volume: 54, Issue:2

    Topics: Breast Neoplasms; Cell Line, Tumor; Cell Membrane; Cell Transformation, Neoplastic; Citric Acid Cycl

2015
MYCN and survivin cooperatively contribute to malignant transformation of fibroblasts.
    Carcinogenesis, 2014, Volume: 35, Issue:2

    Topics: Adenosine Triphosphate; Animals; Apoptosis; Blotting, Western; Cell Hypoxia; Cell Proliferation; Cel

2014
Blocking lactate export by inhibiting the Myc target MCT1 Disables glycolysis and glutathione synthesis.
    Cancer research, 2014, Feb-01, Volume: 74, Issue:3

    Topics: Animals; Cell Death; Cell Line, Tumor; Cell Proliferation; Cell Transformation, Neoplastic; Cluster

2014
Ras-induced epigenetic inactivation of the RRAD (Ras-related associated with diabetes) gene promotes glucose uptake in a human ovarian cancer model.
    The Journal of biological chemistry, 2014, May-16, Volume: 289, Issue:20

    Topics: Adult; Aged; Animals; Biological Transport; Carcinogenesis; Cell Line, Tumor; Cell Transformation, N

2014
Plk1 phosphorylation of PTEN causes a tumor-promoting metabolic state.
    Molecular and cellular biology, 2014, Oct-01, Volume: 34, Issue:19

    Topics: Animals; Antineoplastic Agents; Benzamides; Cell Cycle Proteins; Cell Line, Tumor; Cell Transformati

2014
Ovarian tumor-initiating cells display a flexible metabolism.
    Experimental cell research, 2014, Oct-15, Volume: 328, Issue:1

    Topics: Animals; Apoptosis; Blotting, Western; Cell Proliferation; Cell Transformation, Neoplastic; Disease

2014
Enhanced anti-tumor immune responses and delay of tumor development in human epidermal growth factor receptor 2 mice immunized with an immunostimulatory peptide in poly(D,L-lactic-co-glycolic) acid nanoparticles.
    Breast cancer research : BCR, 2015, Mar-31, Volume: 17

    Topics: Animals; Antigen Presentation; Breast Neoplasms; Cancer Vaccines; Cell Transformation, Neoplastic; D

2015
Glutamine promotes ovarian cancer cell proliferation through the mTOR/S6 pathway.
    Endocrine-related cancer, 2015, Volume: 22, Issue:4

    Topics: Adenosine Triphosphate; Apoptosis; Cell Cycle; Cell Line, Tumor; Cell Proliferation; Cell Transforma

2015
TNFR1 Regulates Ovarian Cancer Cell Tumorigenicity Through PIK3CB-p110Beta.
    Current molecular medicine, 2015, Volume: 15, Issue:5

    Topics: Animals; Cell Line, Tumor; Cell Transformation, Neoplastic; Class I Phosphatidylinositol 3-Kinases;

2015
A novel perfused Bloch-McConnell simulator for analyzing the accuracy of dynamic hyperpolarized MRS.
    Medical physics, 2016, Volume: 43, Issue:2

    Topics: Animals; Cell Transformation, Neoplastic; Lactic Acid; Magnetic Resonance Spectroscopy; Mice; Models

2016
Transformation by different oncogenes relies on specific metabolic adaptations.
    Cell cycle (Georgetown, Tex.), 2016, Volume: 15, Issue:19

    Topics: Adaptation, Physiological; Animals; Breast Neoplasms; Cell Respiration; Cell Transformation, Neoplas

2016
SBDS-Deficient Cells Have an Altered Homeostatic Equilibrium due to Translational Inefficiency Which Explains their Reduced Fitness and Provides a Logical Framework for Intervention.
    PLoS genetics, 2017, Volume: 13, Issue:1

    Topics: Adenosine Triphosphate; Animals; Cell Line; Cell Transformation, Neoplastic; DNA Damage; Fibroblasts

2017
Lactaturia and loss of sodium-dependent lactate uptake in the colon of SLC5A8-deficient mice.
    The Journal of biological chemistry, 2008, Sep-05, Volume: 283, Issue:36

    Topics: Animals; Butyrates; Carcinogens; Cation Transport Proteins; Cell Transformation, Neoplastic; Colon;

2008
Detection of metabolic alterations in non-tumor gastrointestinal tissue of the Apc(Min/+) mouse by (1)H MAS NMR spectroscopy.
    Journal of proteome research, 2009, Volume: 8, Issue:3

    Topics: Adenomatous Polyposis Coli Protein; Animals; Cell Transformation, Neoplastic; Colon; Dimethylamines;

2009
Increased OXPHOS activity precedes rise in glycolytic rate in H-RasV12/E1A transformed fibroblasts that develop a Warburg phenotype.
    Molecular cancer, 2009, Jul-31, Volume: 8

    Topics: Adenovirus E1A Proteins; Animals; Cell Line, Transformed; Cell Proliferation; Cell Transformation, N

2009
Warburg effect revisited: an epigenetic link between glycolysis and gastric carcinogenesis.
    Oncogene, 2010, Jan-21, Volume: 29, Issue:3

    Topics: Aged; Animals; Cell Line, Tumor; Cell Transformation, Neoplastic; DNA Methylation; Down-Regulation;

2010
Fluorescent, superparamagnetic nanospheres for drug storage, targeting, and imaging: a multifunctional nanocarrier system for cancer diagnosis and treatment.
    ACS nano, 2010, Sep-28, Volume: 4, Issue:9

    Topics: Animals; Cell Line, Tumor; Cell Transformation, Neoplastic; Drug Carriers; Fluorescent Dyes; Humans;

2010
CD147 subunit of lactate/H+ symporters MCT1 and hypoxia-inducible MCT4 is critical for energetics and growth of glycolytic tumors.
    Proceedings of the National Academy of Sciences of the United States of America, 2011, Oct-04, Volume: 108, Issue:40

    Topics: Basigin; Cell Line, Tumor; Cell Proliferation; Cell Transformation, Neoplastic; DNA Primers; Flow Cy

2011
The metabolic profile of tumors depends on both the responsible genetic lesion and tissue type.
    Cell metabolism, 2012, Feb-08, Volume: 15, Issue:2

    Topics: Animals; Blotting, Western; Cell Line, Tumor; Cell Transformation, Neoplastic; Citric Acid Cycle; DN

2012
Metabolic reprogramming of cancer-associated fibroblasts by TGF-β drives tumor growth: connecting TGF-β signaling with "Warburg-like" cancer metabolism and L-lactate production.
    Cell cycle (Georgetown, Tex.), 2012, Aug-15, Volume: 11, Issue:16

    Topics: Animals; Autocrine Communication; Autophagy; Breast Neoplasms; Caveolin 1; Cell Line, Tumor; Cell Tr

2012
Mitochondrial fission induces glycolytic reprogramming in cancer-associated myofibroblasts, driving stromal lactate production, and early tumor growth.
    Oncotarget, 2012, Volume: 3, Issue:8

    Topics: Adenosine Triphosphate; Autophagy; Cell Line, Tumor; Cell Transformation, Neoplastic; Energy Metabol

2012
The consequences of enhanced cell-autonomous glucose metabolism.
    Trends in endocrinology and metabolism: TEM, 2012, Volume: 23, Issue:11

    Topics: Animals; Biological Transport; Cell Transformation, Neoplastic; Glucose; Glycolysis; Humans; Lactic

2012
Withaferin A suppresses tumor promoter 12-O-tetradecanoylphorbol 13-acetate-induced decreases in isocitrate dehydrogenase 1 activity and mitochondrial function in skin epidermal JB6 cells.
    Cancer science, 2013, Volume: 104, Issue:2

    Topics: Animals; Cell Line, Tumor; Cell Proliferation; Cell Respiration; Cell Transformation, Neoplastic; Do

2013
EGFR-induced and PKCε monoubiquitylation-dependent NF-κB activation upregulates PKM2 expression and promotes tumorigenesis.
    Molecular cell, 2012, Dec-14, Volume: 48, Issue:5

    Topics: Animals; Brain Neoplasms; Carrier Proteins; Cell Line, Tumor; Cell Transformation, Neoplastic; Enzym

2012
1H HR-MAS NMR spectroscopy of tumor-induced local metabolic "field-effects" enables colorectal cancer staging and prognostication.
    Journal of proteome research, 2013, Feb-01, Volume: 12, Issue:2

    Topics: Adenocarcinoma; Adult; Aged; Aged, 80 and over; Amino Acids; Biomarkers, Tumor; Cell Transformation,

2013
p58(IPK)-mediated attenuation of the proapoptotic PERK-CHOP pathway allows malignant progression upon low glucose.
    Molecular cell, 2013, Mar-28, Volume: 49, Issue:6

    Topics: Acetylgalactosamine; Animals; Apoptosis; Cell Hypoxia; Cell Line; Cell Proliferation; Cell Transform

2013
The role of hypoxia-inducible signaling pathway in nickel carcinogenesis.
    Environmental health perspectives, 2002, Volume: 110 Suppl 5

    Topics: Animals; Cell Cycle Proteins; Cell Hypoxia; Cell Transformation, Neoplastic; Disease Progression; DN

2002
[Decreasing the risk of developing colorectal carcinoma. Lactic acid forming bacteria].
    Krankenpflege Journal, 2003, Volume: 41, Issue:7-9

    Topics: Animals; Bifidobacterium; Cell Transformation, Neoplastic; Clinical Trials as Topic; Colorectal Neop

2003
Ras-dependent carbon metabolism and transformation in mouse fibroblasts.
    Oncogene, 2006, Aug-31, Volume: 25, Issue:39

    Topics: Animals; Apoptosis; Cell Cycle; Cell Death; Cell Transformation, Neoplastic; Cells, Cultured; Enzyme

2006
Attenuation of LDH-A expression uncovers a link between glycolysis, mitochondrial physiology, and tumor maintenance.
    Cancer cell, 2006, Volume: 9, Issue:6

    Topics: Adenosine Triphosphate; Animals; Cell Hypoxia; Cell Line, Tumor; Cell Proliferation; Cell Transforma

2006
Transformation of human mesenchymal stem cells increases their dependency on oxidative phosphorylation for energy production.
    Proceedings of the National Academy of Sciences of the United States of America, 2007, Apr-10, Volume: 104, Issue:15

    Topics: Adenosine Triphosphate; Adult; Blotting, Western; Cell Transformation, Neoplastic; Energy Metabolism

2007
[Biodistribution of (99m)Tc-labeled anti-VEGF mAb 5-FU loaded polylactic acid nanoparticles in human gastric carcinoma xenografts].
    Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2007, Volume: 27, Issue:8

    Topics: Animals; Antibodies, Monoclonal; Cell Line, Tumor; Cell Transformation, Neoplastic; Female; Fluorour

2007
p53 regulates glucose metabolism through an IKK-NF-kappaB pathway and inhibits cell transformation.
    Nature cell biology, 2008, Volume: 10, Issue:5

    Topics: Animals; Cell Transformation, Neoplastic; Cells, Cultured; Fibroblasts; Genes, ras; Glucose; Glucose

2008
Regulation of prolyl hydroxylase activity in L-929 cells by mechanisms unrelated to glycolytic metabolism.
    Collagen and related research, 1984, Volume: 4, Issue:5

    Topics: Animals; Ascorbic Acid; Cell Line; Cell Transformation, Neoplastic; Enzyme Activation; Glycolysis; L

1984
Effects of pyruvate on the growth of normal and transformed hamster embryo fibroblasts.
    Journal of cellular physiology, 1982, Volume: 110, Issue:3

    Topics: Animals; Cell Division; Cell Line; Cell Transformation, Neoplastic; Cell Transformation, Viral; Cric

1982
Lactate-mediated changes in growth morphology and transformation frequency of irradiated C3H 10T1/2 cells.
    Cell biology international reports, 1983, Volume: 7, Issue:11

    Topics: Animals; Cell Division; Cell Line; Cell Survival; Cell Transformation, Neoplastic; Clone Cells; Embr

1983
Ultrastructural differences between control and nitrosomethylurea-transformed cells of rat hepatocyte origin.
    Experimental cell research, 1982, Volume: 138, Issue:2

    Topics: Animals; Cell Line; Cell Nucleus; Cell Transformation, Neoplastic; Cytoplasm; Cytoplasmic Granules;

1982
Liver calcium homeostasis modification by iron: a probable factor in its carcinogenesis.
    Neoplasma, 1994, Volume: 41, Issue:4

    Topics: Adenosine Triphosphate; Animals; Calcium; Calcium Radioisotopes; Cell Transformation, Neoplastic; Fe

1994
Primary hepatocytes outperform Hep G2 cells as the source of biotransformation functions in a bioartificial liver.
    Annals of surgery, 1994, Volume: 220, Issue:1

    Topics: Albumins; Animals; Artificial Organs; Biotransformation; Cell Line, Transformed; Cell Transformation

1994
Increased choline signal coinciding with malignant degeneration of cerebral gliomas: a serial proton magnetic resonance spectroscopy imaging study.
    Journal of neurosurgery, 1997, Volume: 87, Issue:4

    Topics: Adult; Aged; Aspartic Acid; Biomarkers, Tumor; Biopsy; Brain Neoplasms; Cell Transformation, Neoplas

1997
Noninvasive evaluation of the malignant potential of intracranial meningiomas performed using proton magnetic resonance spectroscopy.
    Journal of neurosurgery, 1999, Volume: 91, Issue:6

    Topics: Adult; Aged; Aged, 80 and over; Antigens, Nuclear; Biomarkers, Tumor; Brain; Cell Division; Cell Tra

1999
Proliferative activity and tumorigenic conversion: impact on cellular metabolism in 3-D culture.
    American journal of physiology. Cell physiology, 2000, Volume: 278, Issue:4

    Topics: Adenosine Triphosphate; Animals; Cell Division; Cell Line, Transformed; Cell Transformation, Neoplas

2000
Reduction in lactate accumulation correlates with differentiation-induced terminal cell division of leukemia cells.
    Differentiation; research in biological diversity, 1991, Volume: 48, Issue:1

    Topics: Acetamides; Animals; Carbon Dioxide; Cell Differentiation; Cell Division; Cell Transformation, Neopl

1991
1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-resistant, flat-cell PC12 variants having a partial loss of transformed phenotype.
    Journal of neurochemistry, 1990, Volume: 55, Issue:2

    Topics: 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; Adrenal Gland Neoplasms; Animals; Cell Transformation,

1990
Acidic cellular environments: activation of latent TGF-beta and sensitization of cellular responses to TGF-beta and EGF.
    International journal of cancer, 1989, May-15, Volume: 43, Issue:5

    Topics: Agar; Animals; Blood; Cell Division; Cell Line; Cell Transformation, Neoplastic; Culture Media; Epid

1989