Page last updated: 2024-10-20

succinic acid and Neoplasms

succinic acid has been researched along with Neoplasms in 33 studies

Succinic Acid: A water-soluble, colorless crystal with an acid taste that is used as a chemical intermediate, in medicine, the manufacture of lacquers, and to make perfume esters. It is also used in foods as a sequestrant, buffer, and a neutralizing agent. (Hawley's Condensed Chemical Dictionary, 12th ed, p1099; McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1851)
succinic acid : An alpha,omega-dicarboxylic acid resulting from the formal oxidation of each of the terminal methyl groups of butane to the corresponding carboxy group. It is an intermediate metabolite in the citric acid cycle.

Neoplasms: New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms.

Research Excerpts

ExcerptRelevanceReference
"Recent reports indicate that cancer-secreted succinate enhances cancer cell migration and promotes cancer metastasis by activating succinate receptor-1 (SUCNR-1)-mediated signaling and transcription pathways."2.82Cancer-derived extracellular succinate: a driver of cancer metastasis. ( Kuo, CC; Wu, JY; Wu, KK, 2022)
"Lysine succinylation is a novel, broad-spectrum, dynamic, non-enzymatic protein post-translational modification (PTM)."2.82A review of the mechanism of succinylation in cancer. ( Han, D; Lu, K, 2022)
"Metabolic reprogramming in cancer cells entails activities that involve several enzymes and metabolites to convert nutrient into building blocks that alter energy metabolism to fuel rapid cell division."2.66Cancer Cell Metabolites: Updates on Current Tracing Methods. ( Maniam, S, 2020)
"In solid tumors, the microenvironment is often immunosuppressive and hypoxic regions are prevalent."2.66Oncometabolites lactate and succinate drive pro-angiogenic macrophage response in tumors. ( Griffioen, AW; Huijbers, EJM; Kes, MMG; Van den Bossche, J, 2020)
"Silencing of PLOD2 expression in breast cancer cells reduced succinate levels and inhibited cancer cell mesenchymal phenotypes and stemness, which was accompanied by elevated 5hmC levels in chromatin."1.91The PLOD2/succinate axis regulates the epithelial-mesenchymal plasticity and cancer cell stemness. ( Chen, J; He, D; Lane, AN; Li, J; Li, L; Qi, Y; Scott, TL; Tong, Y; Wang, C; Xiong, G; Xu, R, 2023)
"Succinic acid is a potential biomarker of SDH related pathologies for diagnostic, evaluation of treatment response and follow-up of the disease."1.72Quantification of succinic acid levels, linked to succinate dehydrogenase (SDH) dysfunctions, by an automated and fully validated liquid chromatography tandem mass spectrometry method suitable for multi-matrix applications. ( Blondel, L; Broutin, S; Lamy, C; Mansard, C; Mercier, L; Paci, A, 2022)
"Here, we established SDHB knockout cancer cell lines from human colon cancer HCT116 cells using the clustered regularly interspaced short palindromic repeat (CRISPR)/Cas9 knockout system, and clarified its metabolic characteristics."1.46Succinate dehydrogenase B-deficient cancer cells are highly sensitive to bromodomain and extra-terminal inhibitors. ( Ando, A; Baba, Y; Ebara, S; Hara, T; Kitazawa, S; Satomi, Y; Soga, T, 2017)
"In exercise, as well as cancer and ischemia, hypoxia-inducible factor 1 (HIF1) transcriptionally activates hundreds of genes vital for cell homeostasis and angiogenesis."1.35Reactive oxygen species regulate hypoxia-inducible factor 1alpha differentially in cancer and ischemia. ( Popel, AS; Qutub, AA, 2008)
"Targeted cancer therapy is a promising strategy for the treatment of this disease."1.33Synthesis and biological evaluation of a paclitaxel immunoconjugate. ( Raisch, KP; Safavy, A, 2005)

Research

Studies (33)

TimeframeStudies, this research(%)All Research%
pre-19905 (15.15)18.7374
1990's2 (6.06)18.2507
2000's2 (6.06)29.6817
2010's12 (36.36)24.3611
2020's12 (36.36)2.80

Authors

AuthorsStudies
Lamy, C1
Mansard, C1
Blondel, L1
Mercier, L1
Paci, A1
Broutin, S1
Elia, I1
Rowe, JH1
Johnson, S1
Joshi, S1
Notarangelo, G1
Kurmi, K1
Weiss, S1
Freeman, GJ1
Sharpe, AH1
Haigis, MC1
Kuo, CC1
Wu, JY1
Wu, KK1
Lu, K4
Han, D3
Liu, Y5
Liu, K1
Thorne, RF1
Shi, R1
Zhang, Q3
Wu, M3
Liu, L3
Tong, Y1
Qi, Y2
Xiong, G1
Li, J8
Scott, TL1
Chen, J2
He, D1
Li, L1
Wang, C4
Lane, AN1
Xu, R1
Chen, F2
Dowerg, B1
Cordes, T1
Maniam, S2
Ning, W1
Xu, H1
Jiang, P1
Cheng, H1
Deng, W1
Guo, Y1
Xue, Y1
Nguépy Keubo, FR1
Mboua, PC1
Djifack Tadongfack, T1
Fokouong Tchoffo, E1
Tasson Tatang, C1
Ide Zeuna, J1
Noupoue, EM1
Tsoplifack, CB1
Folefack, GO1
Kettani, M1
Bandelier, P1
Huo, J1
Li, H4
Yu, D1
Arulsamy, N1
AlAbbad, S1
Sardot, T1
Lekashvili, O1
Decato, D1
Lelj, F1
Alexander Ross, JB1
Rosenberg, E1
Nazir, H1
Muthuswamy, N1
Louis, C1
Jose, S1
Prakash, J1
Buan, MEM1
Flox, C1
Chavan, S1
Shi, X1
Kauranen, P1
Kallio, T1
Maia, G1
Tammeveski, K1
Lymperopoulos, N1
Carcadea, E1
Veziroglu, E1
Iranzo, A1
M Kannan, A1
Arunamata, A1
Tacy, TA1
Kache, S1
Mainwaring, RD1
Ma, M1
Maeda, K1
Punn, R1
Noguchi, S1
Hahn, S3
Iwasa, Y3
Ling, J2
Voccio, JP2
Kim, Y3
Song, J3
Bascuñán, J2
Chu, Y1
Tomita, M1
Cazorla, M1
Herrera, E1
Palomeque, E1
Saud, N1
Hoplock, LB1
Lobchuk, MM1
Lemoine, J1
Li, X11
Henson, MA1
Unsihuay, D1
Qiu, J1
Swaroop, S1
Nagornov, KO1
Kozhinov, AN1
Tsybin, YO1
Kuang, S1
Laskin, J1
Zin, NNINM1
Mohamad, MN1
Roslan, K1
Abdul Wafi, S1
Abdul Moin, NI1
Alias, A1
Zakaria, Y1
Abu-Bakar, N1
Naveed, A1
Jilani, K1
Siddique, AB1
Akbar, M1
Riaz, M1
Mushtaq, Z1
Sikandar, M1
Ilyas, S1
Bibi, I1
Asghar, A1
Rasool, G1
Irfan, M1
Li, XY1
Zhao, S1
Fan, XH1
Chen, KP1
Hua, W1
Liu, ZM1
Xue, XD1
Zhou, B1
Zhang, S2
Xing, YL1
Chen, MA1
Sun, Y1
Neradilek, MB1
Wu, XT1
Zhang, D2
Huang, W1
Cui, Y1
Yang, QQ1
Li, HW1
Zhao, XQ1
Hossein Rashidi, B1
Tarafdari, A1
Ghazimirsaeed, ST1
Shahrokh Tehraninezhad, E1
Keikha, F1
Eslami, B1
Ghazimirsaeed, SM1
Jafarabadi, M1
Silvani, Y1
Lovita, AND1
Maharani, A1
Wiyasa, IWA1
Sujuti, H1
Ratnawati, R1
Raras, TYM1
Lemin, AS1
Rahman, MM1
Pangarah, CA1
Kiyu, A1
Zeng, C2
Du, H1
Lin, D1
Jalan, D1
Rubagumya, F1
Hopman, WM1
Vanderpuye, V1
Lopes, G1
Seruga, B1
Booth, CM1
Berry, S1
Hammad, N1
Sajo, EA1
Okunade, KS1
Olorunfemi, G1
Rabiu, KA1
Anorlu, RI1
Xu, C2
Xiang, Y1
Xu, X1
Zhou, L2
Dong, X1
Tang, S1
Gao, XC1
Wei, CH1
Zhang, RG1
Cai, Q1
He, Y1
Tong, F1
Dong, JH1
Wu, G1
Dong, XR1
Tang, X1
Tao, F1
Xiang, W1
Zhao, Y2
Jin, L1
Tao, H1
Lei, Y1
Gan, H1
Huang, Y1
Chen, Y3
Chen, L3
Shan, A1
Zhao, H2
Ma, Q1
Wang, J4
Zhang, E1
Zhang, J3
Li, Y5
Xue, F1
Deng, L1
Yan, Z2
Wang, Y2
Meng, J1
Chen, G2
Anastassiadou, M1
Bernasconi, G1
Brancato, A1
Carrasco Cabrera, L1
Greco, L1
Jarrah, S1
Kazocina, A1
Leuschner, R1
Magrans, JO1
Miron, I1
Nave, S1
Pedersen, R1
Reich, H1
Rojas, A1
Sacchi, A1
Santos, M1
Theobald, A1
Vagenende, B1
Verani, A1
Du, L1
Liu, X1
Ren, Y1
Li, P1
Jiao, Q1
Meng, P1
Wang, F2
Wang, YS1
Zhou, X2
Wang, W1
Wang, S2
Hou, J1
Zhang, A1
Lv, B1
Gao, C1
Pang, D1
Ahmad, NH1
Wang, L1
Zhu, J2
Zhang, L2
Zhuang, T1
Tu, J1
Zhao, Z1
Qu, Y1
Yao, H1
Wang, X5
Lee, DF1
Shen, J3
Wen, L1
Huang, G2
Xie, X1
Zhao, Q1
Hu, W1
Zhang, Y4
Wu, X1
Lu, J2
Li, M1
Li, W2
Wu, W1
Du, F1
Ji, H1
Yang, X2
Xu, Z1
Wan, L1
Wen, Q1
Cho, CH1
Zou, C1
Xiao, Z1
Liao, J1
Su, X1
Bi, Z1
Su, Q1
Huang, H1
Wei, Y2
Gao, Y2
Na, KJ1
Choi, H1
Oh, HR1
Kim, YH1
Lee, SB1
Jung, YJ1
Koh, J1
Park, S1
Lee, HJ1
Jeon, YK1
Chung, DH1
Paeng, JC1
Park, IK1
Kang, CH1
Cheon, GJ1
Kang, KW1
Lee, DS1
Kim, YT1
Pajuelo-Lozano, N1
Alcalá, S1
Sainz, B1
Perona, R1
Sanchez-Perez, I1
Logotheti, S1
Marquardt, S1
Gupta, SK1
Richter, C1
Edelhäuser, BAH1
Engelmann, D1
Brenmoehl, J1
Söhnchen, C1
Murr, N1
Alpers, M1
Singh, KP1
Wolkenhauer, O1
Heckl, D1
Spitschak, A1
Pützer, BM1
Liao, Y1
Cheng, J1
Kong, X1
Li, S2
Zhang, M4
Zhang, H1
Yang, T2
Dong, Y1
Xu, Y1
Yuan, Z1
Cao, J2
Zheng, Y1
Luo, Z1
Mei, Z1
Yao, Y1
Liu, Z2
Liang, C1
Yang, H1
Song, Y1
Yu, K1
Zhu, C1
Huang, Z1
Qian, J1
Ge, J1
Hu, J2
Wang, H2
Mi, Y1
Kong, H1
Xi, D1
Yan, W2
Luo, X1
Ning, Q1
Chang, X2
Zhang, T2
Wang, Q2
Rathore, MG1
Reddy, K1
Chen, H1
Shin, SH1
Ma, WY1
Bode, AM1
Dong, Z1
Mu, W1
Liu, C3
Gao, F1
Lu, H1
Zhang, X4
Cai, X1
Ji, RY1
Hou, Y3
Tian, J3
Shi, Y1
Ying, S1
Tan, M1
Feng, G1
Kuang, Y1
Chen, D1
Wu, D3
Zhu, ZQ1
Tang, HX1
Shi, ZE1
Kang, J1
Liu, Q1
Qi, J2
Mu, J1
Cong, Z1
Chen, S2
Fu, D1
Li, Z2
Celestrin, CP1
Rocha, GZ1
Stein, AM1
Guadagnini, D1
Tadelle, RM1
Saad, MJA1
Oliveira, AG1
Bianconi, V1
Bronzo, P1
Banach, M1
Sahebkar, A1
Mannarino, MR1
Pirro, M1
Patsourakos, NG1
Kouvari, M1
Kotidis, A1
Kalantzi, KI1
Tsoumani, ME1
Anastasiadis, F1
Andronikos, P1
Aslanidou, T1
Efraimidis, P1
Georgiopoulos, A1
Gerakiou, K1
Grigoriadou-Skouta, E1
Grigoropoulos, P1
Hatzopoulos, D1
Kartalis, A1
Lyras, A1
Markatos, G1
Mikrogeorgiou, A1
Myroforou, I1
Orkopoulos, A1
Pavlidis, P1
Petras, C1
Riga, M1
Skouloudi, M1
Smyrnioudis, N1
Thomaidis, K1
Tsikouri, GE1
Tsikouris, EI1
Zisimos, K1
Vavoulis, P1
Vitali, MG1
Vitsas, G1
Vogiatzidis, C1
Chantanis, S1
Fousas, S1
Panagiotakos, DB1
Tselepis, AD1
Jungen, C1
Alken, FA1
Eickholt, C1
Scherschel, K1
Kuklik, P1
Klatt, N1
Schwarzl, J1
Moser, J1
Jularic, M1
Akbulak, RO1
Schaeffer, B1
Willems, S1
Meyer, C1
Nowak, JK1
Szczepanik, M1
Trypuć, M1
Pogorzelski, A1
Bobkowski, W1
Grytczuk, M1
Minarowska, A1
Wójciak, R1
Walkowiak, J1
Lu, Y1
Xi, J1
Li, C1
Chen, W2
Hu, X1
Zhang, F1
Wei, H1
Wang, Z1
Gurzu, S1
Jung, I1
Sugimura, H2
Stefan-van Staden, RI1
Yamada, H1
Natsume, H1
Iwashita, Y1
Szodorai, R1
Szederjesi, J1
Yari, D1
Ehsanbakhsh, Z1
Validad, MH1
Langroudi, FH1
Esfandiari, H1
Prager, A1
Hassanpour, K1
Kurup, SP1
Mets-Halgrimson, R1
Yoon, H1
Zeid, JL1
Mets, MB1
Rahmani, B1
Araujo-Castillo, RV1
Culquichicón, C1
Solis Condor, R1
Efendi, F1
Sebayang, SK1
Astutik, E1
Hadisuyatmana, S1
Has, EMM1
Kuswanto, H1
Foroutan, T1
Ahmadi, F1
Moayer, F1
Khalvati, S1
Lyu, Y1
Huang, J1
Yu, N1
Wen, Z1
Hou, H1
Zhao, T1
Gupta, A1
Khosla, N1
Govindasamy, V1
Saini, A1
Annapurna, K1
Dhakate, SR1
Akkaya, Ö1
Chandgude, AL1
Dömling, A1
Harnett, J1
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Carè, J1
Leach, M1
Brown, D1
Cramer, H1
Pinder, TA1
Steel, A1
Anheyer, D1
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Flores, K1
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Valdes, C1
Lopez, J1
Padilla, V1
Alcoutlabi, M1
Parsons, J1
Núñez, K1
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Bruce, D1
Thevenot, P1
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Gonçalves, H1
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Jarvis, D1
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Nakajima, K1
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Raucci, U1
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Martínez, TJ1
Mordi, NA1
Mordi, IR1
Singh, JS1
McCrimmon, RJ1
Struthers, AD1
Lang, CC1
Wang, XW1
Yuan, LJ1
Yang, Y1
Chen, WF1
Luo, R1
Yang, K1
Amarasiri, SS1
Attanayake, AP1
Arawwawala, LDAM1
Jayatilaka, KAPW1
Mudduwa, LKB1
Ogunsuyi, O2
Akanni, O1
Alabi, O1
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Shah, A1
Begum, R1
Song, H2
Lian, Y1
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Skipper, MT1
Hvas, AM1
Larsen, OH1
Hijazi, Z1
Granger, CB1
Hohnloser, SH1
Westerbergh, J1
Lindbäck, J1
Alexander, JH1
Keltai, M1
Parkhomenko, A1
López-Sendón, JL1
Lopes, RD1
Siegbahn, A1
Wallentin, L1
El-Tarabany, MS1
Saleh, AA1
El-Araby, IE1
El-Magd, MA1
van Ginkel, MPH1
Schijven, MP1
van Grevenstein, WMU1
Schreuder, HWR1
Pereira, EDM1
da Silva, J1
Carvalho, PDS1
Grivicich, I1
Picada, JN1
Salgado Júnior, IB1
Vasques, GJ1
Pereira, MADS1
Reginatto, FH1
Ferraz, ABF1
Vasilenko, EA1
Gorshkova, EN1
Astrakhantseva, IV1
Drutskaya, MS1
Tillib, SV1
Nedospasov, SA1
Mokhonov, VV1
Nam, YW1
Cui, M1
Orfali, R1
Viegas, A1
Nguyen, M1
Mohammed, EHM1
Zoghebi, KA1
Rahighi, S1
Parang, K1
Patterson, KC1
Kahanovitch, U1
Gonçalves, CM1
Hablitz, JJ1
Staruschenko, A1
Mulkey, DK1
Olsen, ML1
Gu, L1
Cao, X1
Mukhtar, A1
Wu, K1
Zhang, YY1
Zhu, Y1
Lu, DZ1
Dong, W1
Bi, WJ1
Feng, XJ1
Wen, LM1
Sun, H1
Qi, MC1
Chang, CC1
Dinh, TK1
Lee, YA1
Wang, FN1
Sung, YC1
Yu, PL1
Chiu, SC1
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Wu, CY1
Huang, YD1
Lu, TT1
Wan, D1
Sakizadeh, J1
Cline, JP1
Snyder, MA1
Kiely, CJ1
McIntosh, S1
Jiang, X1
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Zhao, CK1
Yang, R1
Zhang, QY1
Chen, KJ2
Liu, H1
He, Z1
Chen, B1
Wu, J1
Du, X1
Moore, J1
Blank, BR1
Eksterowicz, J1
Sutimantanapi, D1
Yuen, N1
Metzger, T1
Chan, B1
Huang, T1
Chen, X1
Duong, F1
Kong, W1
Chang, JH1
Sun, J1
Zavorotinskaya, T1
Ye, Q1
Junttila, MR1
Ndubaku, C1
Friedman, LS1
Fantin, VR1
Sun, D1
Fei, P1
Xie, Q1
Jiang, Y1
Feng, H1
Chang, Y1
Kang, H1
Xing, M1
Shao, Z1
Yuan, C1
Wu, Y1
Allan, R1
Canham, K1
Wallace, R1
Singh, D1
Ward, J1
Cooper, A1
Newcomb, C1
Nammour, S1
El Mobadder, M1
Maalouf, E1
Namour, M1
Namour, A1
Rey, G1
Matamba, P1
Matys, J1
Zeinoun, T1
Grzech-Leśniak, K1
Segabinazi Peserico, C1
Garozi, L1
Zagatto, AM1
Machado, FA1
Hirth, JM1
Dinehart, EE1
Lin, YL1
Kuo, YF1
Nouri, SS1
Ritchie, C1
Volow, A1
Li, B2
McSpadden, S1
Dearman, K1
Kotwal, A1
Sudore, RL1
Ward, L1
Thakur, A1
Kondadasula, SV1
Ji, K1
Schalk, DL1
Bliemeister, E1
Ung, J1
Aboukameel, A1
Casarez, E1
Sloane, BF1
Lum, LG1
Xiao, M1
Feng, X1
Gao, R1
Du, B1
Brooks, T1
Zwirner, J1
Hammer, N1
Ondruschka, B1
Jermy, M1
Luengo, A1
Marzo, I1
Reback, M1
Daubit, IM1
Fernández-Moreira, V1
Metzler-Nolte, N1
Gimeno, MC1
Tonchev, I1
Heberman, D1
Peretz, A1
Medvedovsky, AT1
Gotsman, I1
Rashi, Y1
Poles, L1
Goland, S1
Perlman, GY1
Danenberg, HD1
Beeri, R1
Shuvy, M1
Fu, Q1
Yang, D1
Sarapulova, A1
Pang, Q1
Meng, Y1
Wei, L1
Ehrenberg, H1
Kim, CC1
Jeong, SH1
Oh, KH1
Nam, KT1
Sun, JY1
Ning, J1
Duan, Z1
Kershaw, SV1
Rogach, AL1
Gao, Z1
Wang, T1
Li, Q1
Cao, T1
Guo, L1
Fu, Y1
Seeger, ZL1
Izgorodina, EI1
Hue, S1
Beldi-Ferchiou, A1
Bendib, I1
Surenaud, M1
Fourati, S1
Frapard, T1
Rivoal, S1
Razazi, K1
Carteaux, G1
Delfau-Larue, MH1
Mekontso-Dessap, A1
Audureau, E1
de Prost, N1
Gao, SS1
Duangthip, D1
Lo, ECM1
Chu, CH1
Roberts, W1
Rosenheck, RA1
Miyake, T1
Kimoto, E1
Luo, L1
Mathialagan, S1
Horlbogen, LM1
Ramanathan, R1
Wood, LS1
Johnson, JG1
Le, VH1
Vourvahis, M1
Rodrigues, AD1
Muto, C1
Furihata, K1
Sugiyama, Y1
Kusuhara, H1
Gong, Q1
Song, W1
Sun, B1
Cao, P1
Gu, S1
Sun, X1
Zhou, G1
Toma, C1
Khandhar, S1
Zalewski, AM1
D'Auria, SJ1
Tu, TM1
Jaber, WA1
Cho, J2
Suwandaratne, NS1
Razek, S1
Choi, YH1
Piper, LFJ1
Watson, DF1
Banerjee, S1
Xie, S1
Lindsay, AP1
Bates, FS1
Lodge, TP1
Hao, Y1
Chapovetsky, A1
Liu, JJ1
Welborn, M1
Luna, JM1
Do, T1
Haiges, R1
Miller Iii, TF1
Marinescu, SC1
Lopez, SA1
Compter, I1
Eekers, DBP1
Hoeben, A1
Rouschop, KMA1
Reymen, B1
Ackermans, L1
Beckervordersantforth, J1
Bauer, NJC1
Anten, MM1
Wesseling, P1
Postma, AA1
De Ruysscher, D1
Lambin, P1
Qiang, L1
Yang, S1
Cui, YH1
He, YY1
Kumar, SK1
Jacobus, SJ1
Cohen, AD1
Weiss, M1
Callander, N1
Singh, AK1
Parker, TL1
Menter, A1
Parsons, B1
Kumar, P1
Kapoor, P1
Rosenberg, A1
Zonder, JA1
Faber, E1
Lonial, S1
Anderson, KC1
Richardson, PG1
Orlowski, RZ1
Wagner, LI1
Rajkumar, SV1
Li, G1
Hou, G1
Cui, J1
Xie, H1
Sun, Z1
Fang, Z1
Dunstand-Guzmán, E1
Hallal-Calleros, C1
Hernández-Velázquez, VM1
Canales-Vargas, EJ1
Domínguez-Roldan, R1
Pedernera, M1
Peña-Chora, G1
Flores-Pérez, I1
Kim, MJ1
Han, C1
White, K1
Park, HJ1
Ding, D1
Boyd, K1
Rothenberger, C1
Bose, U1
Carmichael, P1
Linser, PJ1
Tanokura, M1
Salvi, R1
Someya, S1
Samuni, A1
Goldstein, S1
Divya, KP1
Dharuman, V1
Feng, J2
Qian, Y1
Cheng, Q1
Ma, H1
Ren, X1
Wei, Q1
Pan, W1
Guo, J1
Situ, B1
An, T1
Zheng, L1
Augusto, S1
Ratola, N1
Tarín-Carrasco, P1
Jiménez-Guerrero, P1
Turco, M1
Schuhmacher, M1
Costa, S1
Teixeira, JP1
Costa, C1
Syed, A1
Marraiki, N1
Al-Rashed, S1
Elgorban, AM1
Yassin, MT1
Chankhanittha, T1
Nanan, S1
Sorokina, KN1
Samoylova, YV1
Gromov, NV1
Ogorodnikova, OL1
Parmon, VN1
Ye, J1
Liao, W1
Zhang, P1
Nabi, M1
Cai, Y1
Li, F1
Alsbou, EM1
Omari, KW1
Adeosun, WA1
Asiri, AM1
Marwani, HM1
Barral, M1
Jemal-Turki, A1
Beuvon, F1
Soyer, P1
Camparo, P1
Cornud, F1
Atwater, BD1
Jones, WS1
Loring, Z1
Friedman, DJ1
Namburath, M1
Papirio, S1
Moscariello, C1
Di Costanzo, N1
Pirozzi, F1
Alappat, BJ1
Sreekrishnan, TR1
Volpin, F1
Woo, YC1
Kim, H1
Freguia, S1
Jeong, N1
Choi, JS1
Phuntsho, S1
Shon, HK1
Domínguez-Zambrano, E1
Pedraza-Chaverri, J1
López-Santos, AL1
Medina-Campos, ON1
Cruz-Rivera, C1
Bueno-Hernández, F1
Espinosa-Cuevas, A1
Bulavaitė, A1
Dalgediene, I1
Michailoviene, V1
Pleckaityte, M1
Sauerbier, P1
Köhler, R1
Renner, G1
Militz, H1
Kes, MMG1
Van den Bossche, J1
Griffioen, AW1
Huijbers, EJM1
Kitazawa, S1
Ebara, S1
Ando, A1
Baba, Y1
Satomi, Y1
Soga, T1
Hara, T1
Du, Y1
Zhang, W1
He, R1
Ismail, M1
Ling, L1
Yao, C1
Fu, Z1
Collins, RRJ1
Patel, K1
Putnam, WC1
Kapur, P1
Rakheja, D1
Schaefer, IM1
Hornick, JL1
Bovée, JVMG1
Ryan, DG1
Murphy, MP1
Frezza, C1
Prag, HA1
Chouchani, ET1
O'Neill, LA2
Mills, EL1
Dalla Pozza, E1
Dando, I1
Pacchiana, R1
Liboi, E1
Scupoli, MT1
Donadelli, M1
Palmieri, M1
Palsson-McDermott, EM1
Hama, S1
Kogure, K1
Tretter, L1
Patocs, A1
Chinopoulos, C1
Jiang, S1
Qutub, AA1
Popel, AS1
Kawamura, A1
Loenarz, C1
Schofield, CJ1
Ralph, SJ1
Moreno-Sánchez, R1
Neuzil, J1
Rodríguez-Enríquez, S1
Cui, S1
Du, C1
Wan, S1
Qian, Z1
Gu, Y1
Chen, WR1
Wang, G1
WOODS, M2
FISCHER, G2
NYHAN, WL1
BUSCH, H1
WENNER, CE1
BLACK, MM1
KLEINER, IS1
Safavy, A1
Raisch, KP1
Norman, DJ1
Kahana, L1
Stuart, FP1
Thistlethwaite, JR1
Shield, CF1
Monaco, A1
Dehlinger, J1
Wu, SC1
Van Horn, A1
Haverty, TP1
Toyoda, K1
Imaida, K1
Mitsumori, K1
Sato, H1
Maekawa, A1
Onodera, H1
Takahashi, M1

Reviews

15 reviews available for succinic acid and Neoplasms

ArticleYear
Cancer-derived extracellular succinate: a driver of cancer metastasis.
    Journal of biomedical science, 2022, Nov-07, Volume: 29, Issue:1

    Topics: Extracellular Space; Humans; Neoplasm Metastasis; Neoplasms; Neovascularization, Pathologic; Paragan

2022
A review of the mechanism of succinylation in cancer.
    Medicine, 2022, Nov-11, Volume: 101, Issue:45

    Topics: Humans; Lysine; Neoplasms; Protein Processing, Post-Translational; Signal Transduction; Succinic Aci

2022
A review of the mechanism of succinylation in cancer.
    Medicine, 2022, Nov-11, Volume: 101, Issue:45

    Topics: Humans; Lysine; Neoplasms; Protein Processing, Post-Translational; Signal Transduction; Succinic Aci

2022
A review of the mechanism of succinylation in cancer.
    Medicine, 2022, Nov-11, Volume: 101, Issue:45

    Topics: Humans; Lysine; Neoplasms; Protein Processing, Post-Translational; Signal Transduction; Succinic Aci

2022
A review of the mechanism of succinylation in cancer.
    Medicine, 2022, Nov-11, Volume: 101, Issue:45

    Topics: Humans; Lysine; Neoplasms; Protein Processing, Post-Translational; Signal Transduction; Succinic Aci

2022
A review of the mechanism of succinylation in cancer.
    Medicine, 2022, Nov-11, Volume: 101, Issue:45

    Topics: Humans; Lysine; Neoplasms; Protein Processing, Post-Translational; Signal Transduction; Succinic Aci

2022
A review of the mechanism of succinylation in cancer.
    Medicine, 2022, Nov-11, Volume: 101, Issue:45

    Topics: Humans; Lysine; Neoplasms; Protein Processing, Post-Translational; Signal Transduction; Succinic Aci

2022
A review of the mechanism of succinylation in cancer.
    Medicine, 2022, Nov-11, Volume: 101, Issue:45

    Topics: Humans; Lysine; Neoplasms; Protein Processing, Post-Translational; Signal Transduction; Succinic Aci

2022
A review of the mechanism of succinylation in cancer.
    Medicine, 2022, Nov-11, Volume: 101, Issue:45

    Topics: Humans; Lysine; Neoplasms; Protein Processing, Post-Translational; Signal Transduction; Succinic Aci

2022
A review of the mechanism of succinylation in cancer.
    Medicine, 2022, Nov-11, Volume: 101, Issue:45

    Topics: Humans; Lysine; Neoplasms; Protein Processing, Post-Translational; Signal Transduction; Succinic Aci

2022
The yin and yang of itaconate metabolism and its impact on the tumor microenvironment.
    Current opinion in biotechnology, 2023, Volume: 84

    Topics: Humans; Neoplasms; Succinates; Succinic Acid; Tumor Microenvironment

2023
Cancer Cell Metabolites: Updates on Current Tracing Methods.
    Chembiochem : a European journal of chemical biology, 2020, 12-11, Volume: 21, Issue:24

    Topics: Amino Acids; Citric Acid; Glucose; Glycine; Humans; Isotope Labeling; Lactic Acid; Neoplasms; Succin

2020
Psychological distress among health care professionals of the three COVID-19 most affected Regions in Cameroon: Prevalence and associated factors.
    Annales medico-psychologiques, 2021, Volume: 179, Issue:2

    Topics: 3' Untranslated Regions; 5'-Nucleotidase; A549 Cells; Accidental Falls; Acetylcholinesterase; Acryli

2021
Oncometabolites lactate and succinate drive pro-angiogenic macrophage response in tumors.
    Biochimica et biophysica acta. Reviews on cancer, 2020, Volume: 1874, Issue:2

    Topics: Angiogenesis Inhibitors; Cell Hypoxia; Cellular Reprogramming; Drug Resistance, Neoplasm; Humans; La

2020
Oncometabolites: A New Paradigm for Oncology, Metabolism, and the Clinical Laboratory.
    Clinical chemistry, 2017, Volume: 63, Issue:12

    Topics: Animals; Clinical Laboratory Services; Fumarates; Glutarates; Humans; Metabolic Networks and Pathway

2017
The role of metabolic enzymes in mesenchymal tumors and tumor syndromes: genetics, pathology, and molecular mechanisms.
    Laboratory investigation; a journal of technical methods and pathology, 2018, Volume: 98, Issue:4

    Topics: Animals; Fumarate Hydratase; Fumarates; Glutarates; Humans; Isocitrate Dehydrogenase; Mixed Function

2018
Coupling Krebs cycle metabolites to signalling in immunity and cancer.
    Nature metabolism, 2019, Volume: 1

    Topics: Citric Acid Cycle; Humans; Immunity, Innate; Macrophages; Neoplasms; Signal Transduction; Succinate

2019
Regulation of succinate dehydrogenase and role of succinate in cancer.
    Seminars in cell & developmental biology, 2020, Volume: 98

    Topics: Animals; Epithelial-Mesenchymal Transition; Humans; Neoplasms; Succinate Dehydrogenase; Succinic Aci

2020
The Warburg effect then and now: from cancer to inflammatory diseases.
    BioEssays : news and reviews in molecular, cellular and developmental biology, 2013, Volume: 35, Issue:11

    Topics: AMP-Activated Protein Kinases; Animals; Carrier Proteins; Cell Line, Tumor; Cell Proliferation; Citr

2013
Nanoparticles consisting of tocopheryl succinate are a novel drug-delivery system with multifaceted antitumor activity.
    Biological & pharmaceutical bulletin, 2014, Volume: 37, Issue:2

    Topics: Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Drug Delivery System

2014
Succinate, an intermediate in metabolism, signal transduction, ROS, hypoxia, and tumorigenesis.
    Biochimica et biophysica acta, 2016, Volume: 1857, Issue:8

    Topics: Carcinogenesis; Gene Expression Regulation, Neoplastic; Humans; Hypoxia; Hypoxia-Inducible Factor 1,

2016
Succinate in the cancer-immune cycle.
    Cancer letters, 2017, 04-01, Volume: 390

    Topics: Citric Acid Cycle; Humans; Inflammation; Neoplasms; Succinic Acid

2017
Inhibitors of succinate: quinone reductase/Complex II regulate production of mitochondrial reactive oxygen species and protect normal cells from ischemic damage but induce specific cancer cell death.
    Pharmaceutical research, 2011, Volume: 28, Issue:11

    Topics: alpha-Tocopherol; Cell Death; Coenzyme A; Dihydrolipoamide Dehydrogenase; Fatty Acids, Nonesterified

2011

Trials

2 trials available for succinic acid and Neoplasms

ArticleYear
Psychological distress among health care professionals of the three COVID-19 most affected Regions in Cameroon: Prevalence and associated factors.
    Annales medico-psychologiques, 2021, Volume: 179, Issue:2

    Topics: 3' Untranslated Regions; 5'-Nucleotidase; A549 Cells; Accidental Falls; Acetylcholinesterase; Acryli

2021
A randomized clinical trial of induction therapy with OKT3 in kidney transplantation.
    Transplantation, 1993, Volume: 55, Issue:1

    Topics: Adolescent; Adult; Aged; Antibody Formation; Azathioprine; Child; Cyclosporine; Drug Administration

1993

Other Studies

17 other studies available for succinic acid and Neoplasms

ArticleYear
Quantification of succinic acid levels, linked to succinate dehydrogenase (SDH) dysfunctions, by an automated and fully validated liquid chromatography tandem mass spectrometry method suitable for multi-matrix applications.
    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2022, Jan-15, Volume: 1189

    Topics: Biomarkers, Tumor; Chromatography, Liquid; Humans; Limit of Detection; Linear Models; Neoplasms; Rep

2022
Tumor cells dictate anti-tumor immune responses by altering pyruvate utilization and succinate signaling in CD8
    Cell metabolism, 2022, 08-02, Volume: 34, Issue:8

    Topics: CD8-Positive T-Lymphocytes; Humans; Immunity; Lactic Acid; Neoplasms; Pyruvate Carboxylase; Pyruvic

2022
Mitochondrial SENP2 regulates the assembly of SDH complex under metabolic stress.
    Cell reports, 2023, 02-28, Volume: 42, Issue:2

    Topics: Cysteine Endopeptidases; Humans; Mitochondria; Mitochondrial Membranes; Molecular Chaperones; Neopla

2023
The PLOD2/succinate axis regulates the epithelial-mesenchymal plasticity and cancer cell stemness.
    Proceedings of the National Academy of Sciences of the United States of America, 2023, 05-16, Volume: 120, Issue:20

    Topics: Cell Line, Tumor; Epithelial Cells; Epithelial-Mesenchymal Transition; Humans; Neoplasms; Procollage

2023
HybridSucc: A Hybrid-learning Architecture for General and Species-specific Succinylation Site Prediction.
    Genomics, proteomics & bioinformatics, 2020, Volume: 18, Issue:2

    Topics: Acylation; Algorithms; Amino Acid Sequence; Area Under Curve; Humans; Lysine; Machine Learning; Neop

2020
Succinate dehydrogenase B-deficient cancer cells are highly sensitive to bromodomain and extra-terminal inhibitors.
    Oncotarget, 2017, Apr-25, Volume: 8, Issue:17

    Topics: Antineoplastic Agents; Azepines; Benzodiazepines; Citric Acid Cycle; CRISPR-Cas Systems; Dehydroepia

2017
Dual 7-ethyl-10-hydroxycamptothecin conjugated phospholipid prodrug assembled liposomes with in vitro anticancer effects.
    Bioorganic & medicinal chemistry, 2017, 06-15, Volume: 25, Issue:12

    Topics: Animals; Antineoplastic Agents, Phytogenic; Camptothecin; Cell Line, Tumor; Cell Survival; Humans; L

2017
Reactive oxygen species regulate hypoxia-inducible factor 1alpha differentially in cancer and ischemia.
    Molecular and cellular biology, 2008, Volume: 28, Issue:16

    Topics: Animals; Ascorbic Acid; Cell Hypoxia; Down-Regulation; Humans; Hydrogen Peroxide; Hypoxia-Inducible

2008
Mutations to metabolic enzymes in cancer herald a need to unify genetics and biochemistry.
    Cell cycle (Georgetown, Tex.), 2011, Sep-01, Volume: 10, Issue:17

    Topics: Citric Acid Cycle; Enzyme Activation; Gene Expression Regulation, Enzymologic; Gene Expression Regul

2011
Targeted cancer therapy with a 2-deoxyglucose-based adriamycin complex.
    Cancer research, 2013, Feb-15, Volume: 73, Issue:4

    Topics: Animals; Antibiotics, Antineoplastic; Cell Line, Tumor; Cell Survival; Chemistry, Pharmaceutical; De

2013
The influence of succinate and 2, 4-dinitrophenol on the respiratory activity of mouse cancers and normal tissues.
    Journal of the National Cancer Institute, 1956, Volume: 17, Issue:5

    Topics: Animals; Dinitrophenols; Mice; Neoplasms; Nitrophenols; Succinates; Succinic Acid

1956
The influence of succinate and 2, 4-dinitrophenol on the respiratory activity of mouse cancers and normal tissues.
    Journal of the National Cancer Institute, 1956, Volume: 17, Issue:5

    Topics: Animals; Dinitrophenols; Mice; Neoplasms; Nitrophenols; Succinates; Succinic Acid

1956
The influence of succinate and 2, 4-dinitrophenol on the respiratory activity of mouse cancers and normal tissues.
    Journal of the National Cancer Institute, 1956, Volume: 17, Issue:5

    Topics: Animals; Dinitrophenols; Mice; Neoplasms; Nitrophenols; Succinates; Succinic Acid

1956
The influence of succinate and 2, 4-dinitrophenol on the respiratory activity of mouse cancers and normal tissues.
    Journal of the National Cancer Institute, 1956, Volume: 17, Issue:5

    Topics: Animals; Dinitrophenols; Mice; Neoplasms; Nitrophenols; Succinates; Succinic Acid

1956
[Succinyldicholine time as qualified diagnostic; further observations on the clinic aspects of succinic acid dicholinester].
    Zentralblatt fur Chirurgie, 1956, Aug-18, Volume: 81, Issue:33

    Topics: Digestive System Surgical Procedures; Neoplasms; Stomach Neoplasms; Succinic Acid; Succinylcholine

1956
[Succinyldicholine time as qualified diagnostic; further observations on the clinic aspects of succinic acid dicholinester].
    Zentralblatt fur Chirurgie, 1956, Aug-18, Volume: 81, Issue:33

    Topics: Digestive System Surgical Procedures; Neoplasms; Stomach Neoplasms; Succinic Acid; Succinylcholine

1956
[Succinyldicholine time as qualified diagnostic; further observations on the clinic aspects of succinic acid dicholinester].
    Zentralblatt fur Chirurgie, 1956, Aug-18, Volume: 81, Issue:33

    Topics: Digestive System Surgical Procedures; Neoplasms; Stomach Neoplasms; Succinic Acid; Succinylcholine

1956
[Succinyldicholine time as qualified diagnostic; further observations on the clinic aspects of succinic acid dicholinester].
    Zentralblatt fur Chirurgie, 1956, Aug-18, Volume: 81, Issue:33

    Topics: Digestive System Surgical Procedures; Neoplasms; Stomach Neoplasms; Succinic Acid; Succinylcholine

1956
Metabolic patterns for succinate-2-C14 in tissues of tumor-bearing rats.
    Cancer research, 1958, Volume: 18, Issue:10

    Topics: Animals; Encephalomyelitis; Neoplasms; Rats; Succinates; Succinic Acid

1958
The oxidation of succinate by ascites tumor cells.
    Archives of biochemistry and biophysics, 1962, Volume: 98

    Topics: Ascites; Biochemical Phenomena; Humans; Metabolism; Neoplasms; Oxidation-Reduction; Succinates; Succ

1962
Succinate stimulation of normal and tumor tissue slice metabolism measured by reduction of tetrazolium chloride.
    Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 1951, Volume: 76, Issue:3

    Topics: Chlorides; Humans; Neoplasms; Succinates; Succinic Acid; Tetrazolium Salts; Tissues

1951
Synthesis and biological evaluation of a paclitaxel immunoconjugate.
    Methods in molecular medicine, 2005, Volume: 109

    Topics: Antibodies, Monoclonal; Apoptosis; Cell Line, Tumor; Cell Proliferation; ErbB Receptors; Humans; Imm

2005
Correlation between cataract and retinopathy due to lighting in F344 rats used in a long-term carcinogenicity study.
    Journal of toxicology and environmental health, 1992, Volume: 37, Issue:4

    Topics: Animals; Animals, Laboratory; Carcinogens; Cataract; Female; Incidence; Light; Lighting; Male; Neopl

1992