JP7267998B2 - 新規ペプチド系癌造影剤 - Google Patents
新規ペプチド系癌造影剤 Download PDFInfo
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- JP7267998B2 JP7267998B2 JP2020509465A JP2020509465A JP7267998B2 JP 7267998 B2 JP7267998 B2 JP 7267998B2 JP 2020509465 A JP2020509465 A JP 2020509465A JP 2020509465 A JP2020509465 A JP 2020509465A JP 7267998 B2 JP7267998 B2 JP 7267998B2
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Description
本発明は、国立衛生研究所によって与えられた助成金番号CA168505、及びP30CA016058によって実施された。政府は、本発明において、ある特定の権利を有する。
本出願は、2017年8月19日出願の米国特許仮出願第62/547,821号の利益を主張し、その全体が参照として本明細書に組み込まれる。
A.定義
本明細書で使用するとき、用語「癌」は、腫瘍などの、制御されない細胞生育又は増殖として定義される。特定の実施形態では、腫瘍は局所浸潤及び転移をもたらす。
本明細書で使用するとき、用語「化学療法剤」は、癌の治療として使用される薬物、毒素、化合物、組成物、又は生物学的実体として定義される。
B.組成物
XR-Z-KR1-LR2 (I)、
式中、
Xは、T、Y、(f)と略されるフルオレニルメチルオキシカルボニル(Fmoc)、4-パラ-ヨード-ベンジル(4Iph)、又は3-ヨードチロシン(3IY)である。Xは、任意の終端残基であってもよい。例えば、Xは、固相ペプチド合成中に使用される固体支持樹脂からの生体適合性自己集合分子の開裂によって生じる化学的部分であり得る。例えば、Xは、アミン、アルコール、アミド基、又はカルボン酸基(例えば、C末端又はN末端のアミノ酸のNH2又はCOOH基)であり得る。あるいは、終端残基Xは、プロピオン酸アミド又はプロピオン酸基であり得る。Xはまた、そのような部分の化学修飾形態(例えば、アルキル化アミン又はエステル化カルボン酸)であってもよい。任意の実施形態では、特に開示されるX、又は、本明細書で企図され、かつ本明細書の開示に包含される変異体は、親油性である。
Zは、HN17のアミノ酸配列、TLPNSNHIKQGL(配列番号1)、HN1-TSPLNIHNGQKL(配列番号2)、HNscr-LNKQTHGLIPNS(配列番号3)、HNJ-NQHSKNTLLIGP(配列番号4)、LKQGNHINLPS(配列番号5)、YSPLNIHNGQKL(配列番号6)、HN18-LPNSNHIKQGL(配列番号7)、YLPNSNHIKQGL(配列番号8)、又はFLPNSNHIKQGL(配列番号9)を表し、
Rは、NR3R4としての末端アミノ基を表し、親油性(例えば、4Iph及びFmocなど)でなければならない。一態様では、親油性物質は、IR800などの両親媒性物質であり得る。
R1は、近赤外蛍光(NIRF)色素(例えば、フルオレセイン(FITC)又は水溶性ジシアニン色素)、又はR2を表す。一態様では、R1はIRDye800(IR800)、又はHであってよい。
R2は、末端CONR5R6を表し、
R3、R4、R5、及びR6は、H、COアルキル(直鎖又は環状)又はCOQR7を表し、
R7は、H、COアルキル(直鎖又は環状)を表し、
Qは、O又はNHR8を表し、
R8は、H、COアルキル(直鎖又は環状)、又はCOXR7を表す。
Rは、例えば、非活性親油性物質、親油性治療薬(例えば、タキソール)、又は1つ以上のCOO-若しくはSO3-基を欠くジシアニンなどの親油性光学色素などの、親油性物質でなければならない。R1及びR2は親水性であり、H若しくはFITCのいずれか、又は診断用の多価光学色素(例えば、光学式手術ナビゲーション又は組織学的組織染色など)m、又は別のペプチド、PKCε、若しくはsiRNAなどの親水性治療薬である。R1及びR2は、異なっていても、又は同じであってもよい。
アミノ酸を表1に分類する。
1.ペプチド
a)HN17及びHN18
b)HN17及びHN18の変異体
c)合成ペプチド
2.コンジュゲート法
3.コンジュゲート
RITCテトラメチルローダミンルソチオシアナート(TetramethylRodaminelsoThioCyanate)、トルーブルー、トルーレッド、ウルトラライト、ウラニンB、ユビテックスSFC、wtGFP、WW781、X-ローダミン、XRITC、キシレンオレンジ、Y66F、Y66H、Y66W、イエローGFP、YFP、YO-PRO-1、YO-PRO-3、YOYO-1、YOYO-3、サイバーグリーン、インドシアニングリーン、チアゾールオレンジ(インターキレーション色素)、量子ドットなどの半導体ナノ粒子、若しくは(光又は他の電磁エネルギー源により活性化することができる)ケージドフルオロフォア、又はこれらの組み合わせが挙げられるが、これらに限定されない。
4.抗酸化剤
5.核酸
a)ヌクレオチド及び関連分子
6.発現系
a)ウイルスプロモーター及びエンハンサー
b)マーカー
7.in vivo撮像
8.内在化ペプチドの単離
9.本開示の方法による癌の検出
10.癌治療
11.放射線治療剤
12.手術
13.化学療法剤
トラーザ(ネシツムマブ)、プララトレキサート、プレドニゾン、プロカルバジン塩酸塩、Proleukin(アルデスロイキン)、Prolia(デノスマブ)、Promacta(エルトロンボパグオラミン)、プロプラノロール塩酸塩、Provenge(シプリューセル-T)、Purinethol(メルカプトプリン)、Purixan(メルカプトプリン)、二塩化ラジウム223、ラロキシフェン塩酸塩、ラムシルマブ、ラスブリカーゼ、R-CHOP、R-CVP、組換えヒトパピローマウイルス(HPV)二価ワクチン、組換えヒトパピローマウイルス(HPV)九価ワクチン、組換えヒトパピローマウイルス(HPV)四価ワクチン、組換えインターフェロンα-2b、レゴラフェニブ、Relistor(メチルナルトレキソン臭化物)、R-EPOCH、レブラミド(レナリドミド)、リウマトレックス(メトトレキサート)、リボシクリブ、R-ICE、リツキサン(リツキシマブ)、Rituxan Hycela(リツキシマブ及びヒアルロニダーゼヒト)、リツキシマブ、リツキシマブ及び、ヒアルロニダーゼヒト、ロラピタント塩酸塩、ロミデプシン、ロミプロスチム、ルビドマイシン(ダウノルビシン塩酸塩)、Rubraca(ルカパリブカンシル酸塩)、ルカパリブカンシル酸塩、ルキソリチニブリン酸塩、Rydapt(ミドスタウリン)、Sclerosol Intrapleural Aerosol(タルク)、シルツキシマブ、シプリューセル-T、ソマチュリンデポ(ランレオチド酢酸塩)、ソニデジブ、ソラフェニブトシル酸塩、スプリセル(ダサチニブ)、STANFORD V、滅菌タルク粉末(タルク)、Steritalc(タルク)、スチバーガ(レゴラフェニブ)、スニチニブリンゴ酸塩、スーテント(スニチニブリンゴ酸塩)、Sylatron(ペグインターフェロンα-2b)、Sylvant(シルツキシマブ)、Synribo(オマセタキシンメペスクシナート)、Tabloid(チオグアニン)、TAC、タフィンラー(ダブラフェニブ)、タグリッソ(オシメルチニブ)、タルク、Talimogene Laherparepvec、タモキシフェンクエン酸塩、Tarabine PFS(シタラビン)、タルセバ(エルロチニブ塩酸塩)、タルグレチン(ベキサロテン)、タシグナ(ニロチニブ)、タキソール(パクリタキセル)、タキソテール(ドセタキセル)、テセントリク、(アテゾリズマブ)、テモダール(テモゾロミド)、テモゾロミド、テムシロリムス、サリドマイド、Thalomid(サリドマイド)、チオグアニン、チオテパ、チサゲンレクロイセル、Tolak(フルオロウラシル--外用)、トポテカン塩酸塩、トレミフェン、トーリセル(テムシロリムス)、トシツモマブ及びヨウ素I131トシツモマブ、Totect(デクスラゾキサン塩酸塩)、TPF、トラベクテジン、トラメチニブ、トラスツズマブ、Treanda(ベンダムスチン塩酸塩)、トリフルリジン及びチピラシル塩酸塩、トリセノックス(三酸化二ヒ素)、タイケルブ(ラパチニブ二トシル酸塩)、Unituxin(ジヌツキシマブ)、ウリジントリアセテート、VAC、バンデタニブ、VAMP、Varubi(ロラピタント塩酸塩)、ベクティビックス(パニツムマブ)、VeIP、Velban(ビンブラスチン硫酸塩)、ベルケイド(ボルテゾミブ)、Velsar(ビンブラスチン硫酸塩)、ベムラフェニブ、Venclexta(ベネトクラクス)、ベネトクラクス、Verzenio(アベマシクリブ)、Viadur(リュープロリド酢酸塩)、Vidaza(アザシチジン)、ビンブラスチン硫酸塩、Vincasar PFS(ビンクリスチン硫酸塩)、ビンクリスチン硫酸塩、ビンクリスチン硫酸塩リポソーム、ビノレルビン酒石酸塩、VIP、ビスモデギブ、Vistogard(ウリジントリアセテート)、Voraxaze(グルカルピダーゼ)、ボリノスタット、ヴォトリエント(パゾパニブ塩酸塩)、Vyxeos(ダウノルビシン塩酸塩及びシタラビンリポソーム)、Wellcovorin(ロイコボリンカルシウム)、ザーコリ(クリゾチニブ)、ゼローダ(カペシタビン)、XELIRI、XELOX、Xgeva(デノスマブ)、ゾーフィゴ(二塩化ラジウム223)、イクスタンジ(エンザルタミド)、ヤーボイ(イピリムマブ)、ヨンデリス(トラベクテジン)、ザルトラップ(ジヴ-アフリベルセプト)、Zarxio(フィルグラスチム)、Zejula(ニラパリブトシル酸塩一水和物)、ゼルボラフ(ベムラフェニブ)、ゼヴァリン(イブリツモマブチウキセタン)、Zinecard(デクスラゾキサン塩酸塩)、ジヴ-アフリベルセプト、ゾフラン(オンダンセトロン塩酸塩)、ゾラデックス(ゴセレリン酢酸塩)、ゾレドロン酸、ゾリンザ(ボリノスタット)、ゾメタ(ゾレドロン酸)、Zydelig(イデラリシブ)、ジカディア(セリチニブ)、及び/又はザイティガ(アビラテロン酢酸塩)が挙げられる。また、本明細書では、PD1/PDL1遮断阻害剤(例えば、ランブロリズマブ、ニボルマブ、ペムブロリズマブ、ピディリズマブ、BMS-936559、アテゾリズマブ、デュルバルマブ、又はアベルマブなど)である化学療法剤も想到される。新生物の治療のため臨床において広く使用されているこれらの化合物は、アドリアマイシンについては21日間隔で、25~75mg/m.sup.2の範囲の用量で静脈内ボーラスで、エトポシドについては35~100mg/m.sup.2で静脈内又は経口的に、投与される。
14.医薬担体/医薬品の送達
a)薬学的に許容される担体
b)治療的使用
15.キット
C.組成物の製造方法
1.ペプチド合成
D.癌を治療する方法
セド二ナトリウム、パージェタ(ペルツズマブ)、ペルツズマブ、Platinol(シスプラチン)、Platinol-AQ(シスプラチン)、プレリキサホル、ポマリドミド、ポマリスト(ポマリドミド)、ポナチニブ塩酸塩、ポートラーザ(ネシツムマブ)、プララトレキサート、プレドニゾン、プロカルバジン塩酸塩、Proleukin(アルデスロイキン)、Prolia(デノスマブ)、Promacta(エルトロンボパグオラミン)、プロプラノロール塩酸塩、Provenge(シプリューセル-T)、Purinethol(メルカプトプリン)、Purixan(メルカプトプリン)、二塩化ラジウム223、ラロキシフェン塩酸塩、ラムシルマブ、ラスブリカーゼ、R-CHOP、R-CVP、組換えヒトパピローマウイルス(HPV)二価ワクチン、組換えヒトパピローマウイルス(HPV)九価ワクチン、組換えヒトパピローマウイルス(HPV)四価ワクチン、組換えインターフェロンα-2b、レゴラフェニブ、Relistor(メチルナルトレキソン臭化物)、R-EPOCH、レブラミド(レナリドミド)、リウマトレックス(メトトレキサート)、リボシクリブ、R-ICE、リツキサン(リツキシマブ)、Rituxan Hycela(リツキシマブ及びヒアルロニダーゼヒト)、リツキシマブ、リツキシマブ及び、ヒアルロニダーゼヒト、ロラピタント塩酸塩、ロミデプシン、ロミプロスチム、ルビドマイシン(ダウノルビシン塩酸塩)、Rubraca(ルカパリブカンシル酸塩)、ルカパリブカンシル酸塩、ルキソリチニブリン酸塩、Rydapt(ミドスタウリン)、Sclerosol Intrapleural Aerosol(タルク)、シルツキシマブ、シプリューセル-T、ソマチュリンデポ(ランレオチド酢酸塩)、ソニデジブ、ソラフェニブトシル酸塩、スプリセル(ダサチニブ)、STANFORD V、滅菌タルク粉末(タルク)、Steritalc(タルク)、スチバーガ(レゴラフェニブ)、スニチニブリンゴ酸塩、スーテント(スニチニブリンゴ酸塩)、Sylatron(ペグインターフェロンα-2b)、Sylvant(シルツキシマブ)、Synribo(オマセタキシンメペスクシナート)、Tabloid(チオグアニン)、TAC、タフィンラー(ダブラフェニブ)、タグリッソ(オシメルチニブ)、タルク、Talimogene Laherparepvec、タモキシフェンクエン酸塩、Tarabine PFS(シタラビン)、タルセバ(エルロチニブ塩酸塩)、タルグレチン(ベキサロテン)、タシグナ(ニロチニブ)、タキソール(パクリタキセル)、タキソテール(ドセタキセル)、テセントリク、(アテゾリズマブ)、テモダール(テモゾロミド)、テモゾロミド、テムシロリムス、サリドマイド、Thalomid(サリドマイド)、チオグアニン、チオテパ、チサゲンレクロイセル、Tolak(フルオロウラシル--外用)、トポテカン塩酸塩、トレミフェン、トーリセル(テムシロリムス)、トシツモマブ及びヨウ素I131トシツモマブ、Totect(デクスラゾキサン塩酸塩)、TPF、トラベクテジン、トラメチニブ、トラスツズマブ、Treanda(ベンダムスチン塩酸塩)、トリフルリジン及びチピラシル塩酸塩、トリセノックス(三酸化二ヒ素)、タイケルブ(ラパチニブ二トシル酸塩)、Unituxin(ジヌツキシマブ)、ウリジントリアセテート、VAC、バンデタニブ、VAMP、Varubi(ロラピタント塩酸塩)、ベクティビックス(パニツムマブ)、VeIP、Velban(ビンブラスチン硫酸塩)、ベルケイド(ボルテゾミブ)、Velsar(ビンブラスチン硫酸塩)、ベムラフェニブ、Venclexta(ベネトクラクス)、ベネトクラクス、Verzenio(アベマシクリブ)、Viadur(リュープロリド酢酸塩)、Vidaza(アザシチジン)、ビンブラスチン硫酸塩、Vincasar PFS(ビンクリスチン硫酸塩)、ビンクリスチン硫酸塩、ビンクリスチン硫酸塩リポソーム、ビノレルビン酒石酸塩、VIP、ビスモデギブ、Vistogard(ウリジントリアセテート)、Voraxaze(グルカルピダーゼ)、ボリノスタット、ヴォトリエント(パゾパニブ塩酸塩)、Vyxeos(ダウノルビシン塩酸塩及びシタラビンリポソーム)、Wellcovorin(ロイコボリンカルシウム)、ザーコリ(クリゾチニブ)、ゼローダ(カペシタビン)、XELIRI、XELOX、Xgeva(デノスマブ)、ゾーフィゴ(二塩化ラジウム223)、イクスタンジ(エンザルタミド)、ヤーボイ(イピリムマブ)、ヨンデリス(トラベクテジン)、ザルトラップ(ジヴ-アフリベルセプト)、Zarxio(フィルグラスチム)、Zejula(ニラパリブトシル酸塩一水和物)、ゼルボラフ(ベムラフェニブ)、ゼヴァリン(イブリツモマブチウキセタン)、Zinecard(デクスラゾキサン塩酸塩)、ジヴ-アフリベルセプト、ゾフラン(オンダンセトロン塩酸塩)、ゾラデックス(ゴセレリン酢酸塩)、ゾレドロン酸、ゾリンザ(ボリノスタット)、ゾメタ(ゾレドロン酸)、Zydelig(イデラリシブ)、ジカディア(セリチニブ)、及び/又はザイティガ(アビラテロン酢酸塩)が挙げられ得るが、これらに限定されない。また、本明細書では、PD1/PDL1遮断阻害剤(例えば、ランブロリズマブ、ニボルマブ、ペムブロリズマブ、ピディリズマブ、BMS-936559、アテゾリズマブ、デュルバルマブ、又はアベルマブなど)である化学療法剤も想到される。
E.実施例
1.実施例1:HN17創薬
a)材料及び方法
(1)材料。
(2)薬剤合成
(3)蛍光標識。
(4)細胞株。
(5)細胞取り込み。
(6)蛍光顕微鏡アッセイ。
(7)in vitro血清安定性。
(8)血液クリアランス。
(9)in vivo撮像。
b)結果
(1)合成及び命名。
(2)in vitro試験。
(3)in vivo試験。
c)考察。
d)結論
2.実施例2:同所性モデルにおける甲状腺髄様癌に対する新規蛍光造影剤の生物学的評価
a)材料及び方法
(1)細胞株の培養:
(2)皮下異種移植片:
(3)近赤外蛍光像:
(4)MTC同所性異種移植片:
(a)細胞調製及び投与プロトコル:
(5)統計分析:
(6)4Iph-HN18-IR800の同所性異種移植片:
b)結果
(1)MTC皮下側腹部異種移植モデルにおける4Iph-HN18-IR800の特性評価
(2)甲状腺髄様癌同所性異種移植片の特徴
(3)MTC同所性モデルにおける4Iph-HN18-IR800の画像化
c)考察
3.実施例3:細胞透過性ペプチドによる細胞膜の直接透過
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Claims (32)
- 腫瘍細胞を標的とする単離ペプチドであって、TLPNSNHIKQGL(配列番号1)、LPNSNHIKQGL(配列番号7)、YLPNSNHIKQGL(配列番号8)、又はFLPNSNHIKQGL(配列番号9)のアミノ酸配列からなる、ペプチド。
- 配列番号1のアミノ酸配列からなる、請求項1に記載のペプチド。
- 配列番号7のアミノ酸配列からなる、請求項1に記載のペプチド。
- アミノ末端アミノ酸に結合した親油性物質を更に含む、請求項1に記載のペプチド。
- 前記親油性物質が、フルオレニルメチルオキシカルボニル、4-パラ-ヨード-ベンジル、4-パラ-ヨード-ベンゾイル、及び/又は3-ヨードチロシンを含む、請求項4に記載のペプチド。
- 前記親油性物質が、フルオレニルメチルオキシカルボニル及び4-パラ-ヨード-ベンジルを含む、請求項5に記載のペプチド。
- 前記ペプチドが、前記腫瘍細胞によって内在化される、請求項1に記載のペプチド。
- a)抗癌剤と、b)腫瘍細胞を標的とするペプチドとを含む医薬組成物であって、前記ペプチドが、TLPNSNHIKQGL(配列番号1)、LPNSNHIKQGL(配列番号7)、YLPNSNHIKQGL(配列番号8)、又はFLPNSNHIKQGL(配列番号9)のアミノ酸配列からなる、医薬組成物。
- 前記ペプチドが配列番号1のアミノ酸配列からなる、請求項8に記載の医薬組成物。
- 前記ペプチドが配列番号7のアミノ酸配列からなる、請求項8に記載の医薬組成物。
- 前記抗癌剤が化学療法剤である、請求項8に記載の医薬組成物。
- 前記抗癌剤が細胞毒性剤である、請求項8に記載の医薬組成物。
- 前記抗癌剤がアポトーシス剤である、請求項8に記載の医薬組成物。
- 前記抗癌剤がDNA損傷剤である、請求項8に記載の医薬組成物。
- 前記抗癌剤が植物アルカロイドである、請求項8に記載の医薬組成物。
- 前記抗癌剤が、放射線増感剤である、請求項8に記載の医薬組成物。
- 前記抗癌剤が、シスプラチン(CDDP)、カルボプラチン、プロカルバジン、メクロレタミン、シクロホスファミド、イホスファミド、メルファラン、クロラムブシル、ブスルファン、ニトロソウレア、ダクチノマイシン、ダウノルビシン、ドキソルビシン、ブレオマイシン、プリカマイシン、マイトマイシン、エトポシド(VP16)、ドセタキセル、セツキシマブ、タモキシフェン、トランスプラチナ、5-フルオロウラシル、ビンクリスチン、ビンブラスチン又はメトトレキサートを含む、請求項8に記載の医薬組成物。
- 前記抗癌剤が、前記ペプチドに共有結合している、請求項17に記載の医薬組成物。
- 前記抗癌剤が、リジン残基において前記ペプチドに共有結合している、請求項18に記載の医薬組成物。
- 前記ペプチドが、アミノ末端アミノ酸に結合した親油性物質を更に含む、請求項8に記載の医薬組成物。
- 前記親油性物質が、フルオレニルメチルオキシカルボニル、4-パラ-ヨード-ベンジル、4-パラ-ヨード-ベンゾイル、及び/又は3-ヨードチロシンを含む、請求項20に記載の医薬組成物。
- 前記親油性物質が、フルオレニルメチルオキシカルボニル(f)及び4-パラ-ヨード-ベンジル(4Iph)を含む、請求項21に記載の医薬組成物。
- 前記ペプチドが、前記腫瘍細胞によって内在化される、請求項8に記載の医薬組成物。
- 検出可能なコンジュゲートを更に含む、請求項8に記載の医薬組成物。
- 前記ペプチドが配列番号1又は配列番号7であり、前記親油性物質が4Iph及びfであり、前記検出可能なコンジュゲートが近赤外蛍光(NIRF)色素である、請求項20または24に記載の医薬組成物。
- 前記ペプチドが配列番号1又は配列番号7であり、前記親油性物質が4Iph及びfであり、前記検出可能なコンジュゲートがInfrared(赤外) 800(IR800)である、請求項20または24に記載の医薬組成物。
- 請求項1~7のいずれか一項に記載のペプチド又は請求項8~26のいずれか一項に記載の医薬組成物を含む、癌細胞を検出するための造影剤。
- 癌を治療するための薬剤の製造における請求項1~7のいずれか一項に記載のペプチド又は請求項8~26のいずれか一項に記載の医薬組成物の使用。
- 請求項1~7のいずれか一項に記載のペプチド又は請求項8~26のいずれか一項に記載の医薬組成物を含む癌細胞の検出剤であって、ここで前記ペプチドが検出可能なコンジュゲートにコンジュゲーションする、癌細胞の検出剤。
- 前記検出可能なコンジュゲートが、シアニン-5(Cy5)、IR800、又はNIRF色素を含む、請求項29に記載の検出剤。
- 前記ペプチドが配列番号1又は配列番号7であり、前記親油性物質が4Iph及びfであり、前記検出可能なコンジュゲートがNIRF色素である、請求項29に記載の検出剤。
- 前記ペプチドが配列番号1又は配列番号7であり、前記親油性物質が4Iph及びfであり、前記検出可能なコンジュゲートがIR800である、請求項29に記載の検出剤。
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EP3668532A4 (en) | 2021-09-01 |
CA3073379A1 (en) | 2019-02-28 |
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CN111225679B (zh) | 2024-03-29 |
WO2019040367A1 (en) | 2019-02-28 |
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