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Monodemethylated polymethoxyflavones from sweet orange (Citrus sinensis) peel inhibit growth of human lung cancer cells by apoptosis

Identifieur interne : 000336 ( PascalFrancis/Corpus ); précédent : 000335; suivant : 000337

Monodemethylated polymethoxyflavones from sweet orange (Citrus sinensis) peel inhibit growth of human lung cancer cells by apoptosis

Auteurs : HANG XIAO ; Chung S. Yang ; SHIMING LI ; HUANYU JIN ; Chi-Tang Ho ; Trusha Patel

Source :

RBID : Pascal:09-0152404

Descripteurs français

English descriptors

Abstract

Polymethoxyflavones (PMFs) are almost exclusively found in the Citrus genus, particularly in the peels of sweet orange (Citrus sinensis L. Osbeck) and mandarin (C. reticulate Blanco). We studied the effects of two major PMFs, namely, nobiletin and 3,5,6,7,8,3',4'-heptamethoxyflavone (HMF), and two major monodemethylated PMFs, namely 5-hydroxy-3,7,8,3',4'-pentamethoxyflavone (5HPMF), and 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone (5HHMF), on the growth of human lung cancer H1299, H441, and H460 cells. Monodemethylated PMFs were much more potent in growth inhibition of lung cancer cells than their permethoxylated counterpart PMFs. In H1299 cells, cell cycle analyses further revealed that monodemethylated PMFs caused significant increase in sub-G0/ Gl phase, suggesting possible role of apoptosis in the growth inhibition observed, whereas the permethoxylated counterpart PMFs did not affect cell cycle distribution at same concentrations tested. These results strongly suggested that the phenolic group is essential for the growth inhibitory activity of monodemethylated PMFs. Further studies in H1299 cells demonstrated that monodemethylated PMFs downregulated oncogenic proteins, such as iNOS, COX-2, Mcl-1, and K-ras, as well as induced apoptosis evidenced by activation of caspase-3 and cleavage of PARP. Our results provide rationale to develop orange peel extract enriched with monodemethylated PMFs into value-added nutraceutical products for cancer prevention.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 1613-4125
A03   1    @0 Mol. nutr. food res. : (Print)
A05       @2 53
A06       @2 3
A08 01  1  ENG  @1 Monodemethylated polymethoxyflavones from sweet orange (Citrus sinensis) peel inhibit growth of human lung cancer cells by apoptosis
A11 01  1    @1 HANG XIAO
A11 02  1    @1 YANG (Chung S.)
A11 03  1    @1 SHIMING LI
A11 04  1    @1 HUANYU JIN
A11 05  1    @1 HO (Chi-Tang)
A11 06  1    @1 PATEL (Trusha)
A14 01      @1 Susan Lehman Cullman Laboratory for Cancer Research, Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey @2 Piscataway, NJ @3 USA @Z 1 aut. @Z 2 aut. @Z 4 aut. @Z 6 aut.
A14 02      @1 Department of Food Science, University of Massachusetts @2 Amherst, MA @3 USA @Z 1 aut.
A14 03      @1 WellGen, Inc @2 North Brunswick, NJ @3 USA @Z 3 aut.
A14 04      @1 Department of Food Science, Rutgers, The State University of New Jersey @2 New Brunswick, NJ @3 USA @Z 5 aut.
A20       @1 398-406
A21       @1 2009
A23 01      @0 ENG
A43 01      @1 INIST @2 9262 @5 354000185540640100
A44       @0 0000 @1 © 2009 INIST-CNRS. All rights reserved.
A45       @0 33 ref.
A47 01  1    @0 09-0152404
A60       @1 P
A61       @0 A
A64 01  1    @0 Molecular nutrition & food research : (Print)
A66 01      @0 DEU
C01 01    ENG  @0 Polymethoxyflavones (PMFs) are almost exclusively found in the Citrus genus, particularly in the peels of sweet orange (Citrus sinensis L. Osbeck) and mandarin (C. reticulate Blanco). We studied the effects of two major PMFs, namely, nobiletin and 3,5,6,7,8,3',4'-heptamethoxyflavone (HMF), and two major monodemethylated PMFs, namely 5-hydroxy-3,7,8,3',4'-pentamethoxyflavone (5HPMF), and 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone (5HHMF), on the growth of human lung cancer H1299, H441, and H460 cells. Monodemethylated PMFs were much more potent in growth inhibition of lung cancer cells than their permethoxylated counterpart PMFs. In H1299 cells, cell cycle analyses further revealed that monodemethylated PMFs caused significant increase in sub-G0/ Gl phase, suggesting possible role of apoptosis in the growth inhibition observed, whereas the permethoxylated counterpart PMFs did not affect cell cycle distribution at same concentrations tested. These results strongly suggested that the phenolic group is essential for the growth inhibitory activity of monodemethylated PMFs. Further studies in H1299 cells demonstrated that monodemethylated PMFs downregulated oncogenic proteins, such as iNOS, COX-2, Mcl-1, and K-ras, as well as induced apoptosis evidenced by activation of caspase-3 and cleavage of PARP. Our results provide rationale to develop orange peel extract enriched with monodemethylated PMFs into value-added nutraceutical products for cancer prevention.
C02 01  X    @0 002A35B11
C02 02  X    @0 002A35B09
C03 01  X  FRE  @0 Bonbon @5 01
C03 01  X  ENG  @0 Sweets @5 01
C03 01  X  SPA  @0 Caramelo @5 01
C03 02  X  FRE  @0 Orange @5 02
C03 02  X  ENG  @0 Orange @5 02
C03 02  X  SPA  @0 Naranja @5 02
C03 03  X  FRE  @0 Citrus sinensis @2 NS @5 10
C03 03  X  ENG  @0 Citrus sinensis @2 NS @5 10
C03 03  X  SPA  @0 Citrus sinensis @2 NS @5 10
C03 04  X  FRE  @0 Pelure @5 19
C03 04  X  ENG  @0 Peel @5 19
C03 04  X  SPA  @0 Cáscara @5 19
C03 05  X  FRE  @0 Croissance @5 20
C03 05  X  ENG  @0 Growth @5 20
C03 05  X  SPA  @0 Crecimiento @5 20
C03 06  X  FRE  @0 Homme @5 24
C03 06  X  ENG  @0 Human @5 24
C03 06  X  SPA  @0 Hombre @5 24
C03 07  X  FRE  @0 Tumeur maligne @2 NM @5 26
C03 07  X  ENG  @0 Malignant tumor @2 NM @5 26
C03 07  X  SPA  @0 Tumor maligno @2 NM @5 26
C07 01  X  FRE  @0 Produit confiserie @5 08
C07 01  X  ENG  @0 Confectionery product @5 08
C07 01  X  SPA  @0 Producto confitería @5 08
C07 02  X  FRE  @0 Rutaceae @2 NS
C07 02  X  ENG  @0 Rutaceae @2 NS
C07 02  X  SPA  @0 Rutaceae @2 NS
C07 03  X  FRE  @0 Dicotyledones @2 NS
C07 03  X  ENG  @0 Dicotyledones @2 NS
C07 03  X  SPA  @0 Dicotyledones @2 NS
C07 04  X  FRE  @0 Angiospermae @2 NS
C07 04  X  ENG  @0 Angiospermae @2 NS
C07 04  X  SPA  @0 Angiospermae @2 NS
C07 05  X  FRE  @0 Spermatophyta @2 NS
C07 05  X  ENG  @0 Spermatophyta @2 NS
C07 05  X  SPA  @0 Spermatophyta @2 NS
C07 06  X  FRE  @0 Cancer @2 NM
C07 06  X  ENG  @0 Cancer @2 NM
C07 06  X  SPA  @0 Cáncer @2 NM
C07 07  X  FRE  @0 Fruit @5 49
C07 07  X  ENG  @0 Fruit @5 49
C07 07  X  SPA  @0 Fruto @5 49
C07 08  X  FRE  @0 Agrume @5 50
C07 08  X  ENG  @0 Citrus fruit @5 50
C07 08  X  SPA  @0 Agrios @5 50
N21       @1 110
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 09-0152404 INIST
ET : Monodemethylated polymethoxyflavones from sweet orange (Citrus sinensis) peel inhibit growth of human lung cancer cells by apoptosis
AU : HANG XIAO; YANG (Chung S.); SHIMING LI; HUANYU JIN; HO (Chi-Tang); PATEL (Trusha)
AF : Susan Lehman Cullman Laboratory for Cancer Research, Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey/Piscataway, NJ/Etats-Unis (1 aut., 2 aut., 4 aut., 6 aut.); Department of Food Science, University of Massachusetts/Amherst, MA/Etats-Unis (1 aut.); WellGen, Inc/North Brunswick, NJ/Etats-Unis (3 aut.); Department of Food Science, Rutgers, The State University of New Jersey/New Brunswick, NJ/Etats-Unis (5 aut.)
DT : Publication en série; Niveau analytique
SO : Molecular nutrition & food research : (Print); ISSN 1613-4125; Allemagne; Da. 2009; Vol. 53; No. 3; Pp. 398-406; Bibl. 33 ref.
LA : Anglais
EA : Polymethoxyflavones (PMFs) are almost exclusively found in the Citrus genus, particularly in the peels of sweet orange (Citrus sinensis L. Osbeck) and mandarin (C. reticulate Blanco). We studied the effects of two major PMFs, namely, nobiletin and 3,5,6,7,8,3',4'-heptamethoxyflavone (HMF), and two major monodemethylated PMFs, namely 5-hydroxy-3,7,8,3',4'-pentamethoxyflavone (5HPMF), and 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone (5HHMF), on the growth of human lung cancer H1299, H441, and H460 cells. Monodemethylated PMFs were much more potent in growth inhibition of lung cancer cells than their permethoxylated counterpart PMFs. In H1299 cells, cell cycle analyses further revealed that monodemethylated PMFs caused significant increase in sub-G0/ Gl phase, suggesting possible role of apoptosis in the growth inhibition observed, whereas the permethoxylated counterpart PMFs did not affect cell cycle distribution at same concentrations tested. These results strongly suggested that the phenolic group is essential for the growth inhibitory activity of monodemethylated PMFs. Further studies in H1299 cells demonstrated that monodemethylated PMFs downregulated oncogenic proteins, such as iNOS, COX-2, Mcl-1, and K-ras, as well as induced apoptosis evidenced by activation of caspase-3 and cleavage of PARP. Our results provide rationale to develop orange peel extract enriched with monodemethylated PMFs into value-added nutraceutical products for cancer prevention.
CC : 002A35B11; 002A35B09
FD : Bonbon; Orange; Citrus sinensis; Pelure; Croissance; Homme; Tumeur maligne
FG : Produit confiserie; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Cancer; Fruit; Agrume
ED : Sweets; Orange; Citrus sinensis; Peel; Growth; Human; Malignant tumor
EG : Confectionery product; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Cancer; Fruit; Citrus fruit
SD : Caramelo; Naranja; Citrus sinensis; Cáscara; Crecimiento; Hombre; Tumor maligno
LO : INIST-9262.354000185540640100
ID : 09-0152404

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Pascal:09-0152404

Le document en format XML

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<div type="abstract" xml:lang="en">Polymethoxyflavones (PMFs) are almost exclusively found in the Citrus genus, particularly in the peels of sweet orange (Citrus sinensis L. Osbeck) and mandarin (C. reticulate Blanco). We studied the effects of two major PMFs, namely, nobiletin and 3,5,6,7,8,3',4'-heptamethoxyflavone (HMF), and two major monodemethylated PMFs, namely 5-hydroxy-3,7,8,3',4'-pentamethoxyflavone (5HPMF), and 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone (5HHMF), on the growth of human lung cancer H1299, H441, and H460 cells. Monodemethylated PMFs were much more potent in growth inhibition of lung cancer cells than their permethoxylated counterpart PMFs. In H1299 cells, cell cycle analyses further revealed that monodemethylated PMFs caused significant increase in sub-G0/ Gl phase, suggesting possible role of apoptosis in the growth inhibition observed, whereas the permethoxylated counterpart PMFs did not affect cell cycle distribution at same concentrations tested. These results strongly suggested that the phenolic group is essential for the growth inhibitory activity of monodemethylated PMFs. Further studies in H1299 cells demonstrated that monodemethylated PMFs downregulated oncogenic proteins, such as iNOS, COX-2, Mcl-1, and K-ras, as well as induced apoptosis evidenced by activation of caspase-3 and cleavage of PARP. Our results provide rationale to develop orange peel extract enriched with monodemethylated PMFs into value-added nutraceutical products for cancer prevention.</div>
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<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Molecular nutrition & food research : (Print)</s0>
</fA64>
<fA66 i1="01">
<s0>DEU</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>Polymethoxyflavones (PMFs) are almost exclusively found in the Citrus genus, particularly in the peels of sweet orange (Citrus sinensis L. Osbeck) and mandarin (C. reticulate Blanco). We studied the effects of two major PMFs, namely, nobiletin and 3,5,6,7,8,3',4'-heptamethoxyflavone (HMF), and two major monodemethylated PMFs, namely 5-hydroxy-3,7,8,3',4'-pentamethoxyflavone (5HPMF), and 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone (5HHMF), on the growth of human lung cancer H1299, H441, and H460 cells. Monodemethylated PMFs were much more potent in growth inhibition of lung cancer cells than their permethoxylated counterpart PMFs. In H1299 cells, cell cycle analyses further revealed that monodemethylated PMFs caused significant increase in sub-G0/ Gl phase, suggesting possible role of apoptosis in the growth inhibition observed, whereas the permethoxylated counterpart PMFs did not affect cell cycle distribution at same concentrations tested. These results strongly suggested that the phenolic group is essential for the growth inhibitory activity of monodemethylated PMFs. Further studies in H1299 cells demonstrated that monodemethylated PMFs downregulated oncogenic proteins, such as iNOS, COX-2, Mcl-1, and K-ras, as well as induced apoptosis evidenced by activation of caspase-3 and cleavage of PARP. Our results provide rationale to develop orange peel extract enriched with monodemethylated PMFs into value-added nutraceutical products for cancer prevention.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002A35B11</s0>
</fC02>
<fC02 i1="02" i2="X">
<s0>002A35B09</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Bonbon</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Sweets</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Caramelo</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Orange</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Orange</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Naranja</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Citrus sinensis</s0>
<s2>NS</s2>
<s5>10</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Citrus sinensis</s0>
<s2>NS</s2>
<s5>10</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Citrus sinensis</s0>
<s2>NS</s2>
<s5>10</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Pelure</s0>
<s5>19</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Peel</s0>
<s5>19</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Cáscara</s0>
<s5>19</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Croissance</s0>
<s5>20</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Growth</s0>
<s5>20</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Crecimiento</s0>
<s5>20</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Homme</s0>
<s5>24</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Human</s0>
<s5>24</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Hombre</s0>
<s5>24</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Tumeur maligne</s0>
<s2>NM</s2>
<s5>26</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Malignant tumor</s0>
<s2>NM</s2>
<s5>26</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Tumor maligno</s0>
<s2>NM</s2>
<s5>26</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Produit confiserie</s0>
<s5>08</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Confectionery product</s0>
<s5>08</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Producto confitería</s0>
<s5>08</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Cancer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Cancer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Cáncer</s0>
<s2>NM</s2>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Fruit</s0>
<s5>49</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Fruit</s0>
<s5>49</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Fruto</s0>
<s5>49</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Agrume</s0>
<s5>50</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Citrus fruit</s0>
<s5>50</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Agrios</s0>
<s5>50</s5>
</fC07>
<fN21>
<s1>110</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 09-0152404 INIST</NO>
<ET>Monodemethylated polymethoxyflavones from sweet orange (Citrus sinensis) peel inhibit growth of human lung cancer cells by apoptosis</ET>
<AU>HANG XIAO; YANG (Chung S.); SHIMING LI; HUANYU JIN; HO (Chi-Tang); PATEL (Trusha)</AU>
<AF>Susan Lehman Cullman Laboratory for Cancer Research, Department of Chemical Biology, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey/Piscataway, NJ/Etats-Unis (1 aut., 2 aut., 4 aut., 6 aut.); Department of Food Science, University of Massachusetts/Amherst, MA/Etats-Unis (1 aut.); WellGen, Inc/North Brunswick, NJ/Etats-Unis (3 aut.); Department of Food Science, Rutgers, The State University of New Jersey/New Brunswick, NJ/Etats-Unis (5 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Molecular nutrition & food research : (Print); ISSN 1613-4125; Allemagne; Da. 2009; Vol. 53; No. 3; Pp. 398-406; Bibl. 33 ref.</SO>
<LA>Anglais</LA>
<EA>Polymethoxyflavones (PMFs) are almost exclusively found in the Citrus genus, particularly in the peels of sweet orange (Citrus sinensis L. Osbeck) and mandarin (C. reticulate Blanco). We studied the effects of two major PMFs, namely, nobiletin and 3,5,6,7,8,3',4'-heptamethoxyflavone (HMF), and two major monodemethylated PMFs, namely 5-hydroxy-3,7,8,3',4'-pentamethoxyflavone (5HPMF), and 5-hydroxy-3,6,7,8,3',4'-hexamethoxyflavone (5HHMF), on the growth of human lung cancer H1299, H441, and H460 cells. Monodemethylated PMFs were much more potent in growth inhibition of lung cancer cells than their permethoxylated counterpart PMFs. In H1299 cells, cell cycle analyses further revealed that monodemethylated PMFs caused significant increase in sub-G0/ Gl phase, suggesting possible role of apoptosis in the growth inhibition observed, whereas the permethoxylated counterpart PMFs did not affect cell cycle distribution at same concentrations tested. These results strongly suggested that the phenolic group is essential for the growth inhibitory activity of monodemethylated PMFs. Further studies in H1299 cells demonstrated that monodemethylated PMFs downregulated oncogenic proteins, such as iNOS, COX-2, Mcl-1, and K-ras, as well as induced apoptosis evidenced by activation of caspase-3 and cleavage of PARP. Our results provide rationale to develop orange peel extract enriched with monodemethylated PMFs into value-added nutraceutical products for cancer prevention.</EA>
<CC>002A35B11; 002A35B09</CC>
<FD>Bonbon; Orange; Citrus sinensis; Pelure; Croissance; Homme; Tumeur maligne</FD>
<FG>Produit confiserie; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Cancer; Fruit; Agrume</FG>
<ED>Sweets; Orange; Citrus sinensis; Peel; Growth; Human; Malignant tumor</ED>
<EG>Confectionery product; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Cancer; Fruit; Citrus fruit</EG>
<SD>Caramelo; Naranja; Citrus sinensis; Cáscara; Crecimiento; Hombre; Tumor maligno</SD>
<LO>INIST-9262.354000185540640100</LO>
<ID>09-0152404</ID>
</server>
</inist>
</record>

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